Canonical Allele Identifier: CA2999693147
Gene: CRYM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21258755C>T , CM000678.2:g.21258755C>T GRCh38
NC_000016.9:g.21270076C>T , CM000678.1:g.21270076C>T GRCh37
NC_000016.8:g.21177577C>T NCBI36
NG_011610.1:g.49342G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000219599.8:c.*26G>A ENSP00000219599.3:n.*26G>A
ENST00000572914.2:c.*26G>A MANE Select ENSP00000461904.2:n.*26G>A
ENST00000219599.7:c.*26G>A ENSP00000219599.3:n.*26G>A
ENST00000543948.5:c.*26G>A ENSP00000440227.1:n.*26G>A
ENST00000570401.5:c.264+34G>A
ENST00000574448.5:c.*520+2499G>A ENSP00000459982.1:n.*520+2499G>A
NM_001888.4:c.*26G>A NP_001879.1:n.*26G>A
XM_011545740.1:c.*26G>A XP_011544042.1:n.*26G>A
XR_950904.1:n.735+3962C>T
XM_024450157.1:c.*26G>A XP_024305925.1:n.*26G>A
NM_001888.5:c.*26G>A NP_001879.1:n.*26G>A
NM_001376256.1:c.*26G>A MANE Select NP_001363185.1:n.*26G>A
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