Canonical Allele Identifier: CA2582641779
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1401204-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401204G>A , CM000681.2:g.1401204G>A GRCh38
NC_000019.9:g.1401203G>A , CM000681.1:g.1401203G>A GRCh37
NC_000019.8:g.1352203G>A NCBI36
NG_009785.1:g.5350C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+92C>T MANE Select ENSP00000252288.1:n.181+92C>T
ENST00000447102.8:c.181+92C>T ENSP00000403536.2:n.181+92C>T
ENST00000640762.1:c.112+161C>T ENSP00000492031.1:n.112+161C>T
ENST00000252288.6:c.181+92C>T ENSP00000252288.1:n.181+92C>T
ENST00000447102.7:c.181+92C>T ENSP00000403536.2:n.181+92C>T
NM_000156.5:c.181+92C>T NP_000147.1:n.181+92C>T
NM_138924.2:c.181+92C>T NP_620279.1:n.181+92C>T
NM_000156.6:c.181+92C>T MANE Select NP_000147.1:n.181+92C>T
NM_138924.3:c.181+92C>T NP_620279.1:n.181+92C>T