Canonical Allele Identifier: CA389037546

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416123G>T , CM000676.2:g.23416123G>T GRCh38
NC_000014.8:g.23885332G>T , CM000676.1:g.23885332G>T GRCh37
NC_000014.7:g.22955172G>T NCBI36
NG_007884.1:g.24539C>A , LRG_384:g.24539C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4834C>A (MYH7) MANE Select ENSP00000347507.3:p.Leu1612Met
ENST00000355349.3:c.4834C>A (MYH7) ENSP00000347507.3:p.Leu1612Met
NM_000257.3:c.4834C>A (MYH7) NP_000248.2:p.Leu1612Met
NR_126491.1:n.384G>T (MHRT)
XM_017021340.1:c.4834C>A (MYH7) XP_016876829.1:p.Leu1612Met
NM_000257.4:c.4834C>A (MYH7) MANE Select NP_000248.2:p.Leu1612Met