Canonical Allele Identifier: CA402996091

Gene: GAMT

Linked Data

• gnomAD v4: 19-1399801-T-A
• MyVariant Identifiers: chr19:g.1399800T>A (hg19) ; chr19:g.1399801T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399801T>A , CM000681.2:g.1399801T>A	GRCh38
NC_000019.9:g.1399800T>A , CM000681.1:g.1399800T>A	GRCh37
NC_000019.8:g.1350800T>A	NCBI36
NG_009785.1:g.6753A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.319A>T MANE Select	ENSP00000252288.1:p.Thr107Ser
ENST00000447102.8:c.319A>T	ENSP00000403536.2:p.Thr107Ser
ENST00000591788.3:c.2A>T
ENST00000640762.1:c.250A>T	ENSP00000492031.1:p.Thr84Ser
ENST00000252288.6:c.319A>T	ENSP00000252288.1:p.Thr107Ser
ENST00000447102.7:c.319A>T	ENSP00000403536.2:p.Thr107Ser
ENST00000591788.2:c.4A>T	ENSP00000466341.2:p.Thr2Ser
NM_000156.5:c.319A>T	NP_000147.1:p.Thr107Ser
NM_138924.2:c.319A>T	NP_620279.1:p.Thr107Ser
NM_000156.6:c.319A>T MANE Select	NP_000147.1:p.Thr107Ser
NM_138924.3:c.319A>T	NP_620279.1:p.Thr107Ser