Canonical Allele Identifier: CA2582641467

Gene: GAMT

Linked Data

• gnomAD v4: 19-1399773-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399774_1399775del , CM000681.2:g.1399774_1399775del	GRCh38
NC_000019.9:g.1399773_1399774del , CM000681.1:g.1399773_1399774del	GRCh37
NC_000019.8:g.1350773_1350774del	NCBI36
NG_009785.1:g.6779_6780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.327+18_327+19del MANE Select	ENSP00000252288.1:n.327+18_327+19del
ENST00000447102.8:c.327+18_327+19del	ENSP00000403536.2:n.327+18_327+19del
ENST00000591788.3:c.10+18_10+19del
ENST00000640762.1:c.258+18_258+19del	ENSP00000492031.1:n.258+18_258+19del
ENST00000252288.6:c.327+18_327+19del	ENSP00000252288.1:n.327+18_327+19del
ENST00000447102.7:c.327+18_327+19del	ENSP00000403536.2:n.327+18_327+19del
ENST00000591788.2:c.12+18_12+19del	ENSP00000466341.2:n.12+18_12+19del
NM_000156.5:c.327+18_327+19del	NP_000147.1:n.327+18_327+19del
NM_138924.2:c.327+18_327+19del	NP_620279.1:n.327+18_327+19del
NM_000156.6:c.327+18_327+19del MANE Select	NP_000147.1:n.327+18_327+19del
NM_138924.3:c.327+18_327+19del	NP_620279.1:n.327+18_327+19del