Canonical Allele Identifier: CA1845640122

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648913A= , CM000671.2:g.34648913A=	GRCh38
NC_000009.11:g.34648910A= , CM000671.1:g.34648910A=	GRCh37
NC_000009.10:g.34638910A=	NCBI36
NG_009029.1:g.7276A=
NG_028966.1:g.1729A=
NG_009029.2:g.7325A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*408+19A=	ENSP00000509954.1:n.*408+19A=
ENST00000378842.8:c.820+19A= MANE Select	ENSP00000368119.4:n.820+19A=
ENST00000378842.7:c.820+19A=	ENSP00000368119.3:n.820+19A=
ENST00000450095.6:c.493+19A=	ENSP00000401956.2:n.493+19A=
ENST00000489643.6:n.900+19A=
ENST00000554085.5:c.*564+19A=	ENSP00000450419.1:n.*564+19A=
ENST00000554550.5:c.*440+19A=	ENSP00000451435.1:n.*440+19A=
ENST00000554638.5:n.1292+19A=
ENST00000555020.5:n.1281+19A=
ENST00000555086.5:n.843A=
ENST00000555754.1:n.184A=
ENST00000556278.1:c.432+457A=	ENSP00000451792.1:n.432+457A=
ENST00000557706.5:n.1395+6A=
NM_000155.3:c.820+19A=	NP_000146.2:n.820+19A=
NM_001258332.1:c.493+19A=	NP_001245261.1:n.493+19A=
NM_000155.4:c.820+19A= MANE Select	NP_000146.2:n.820+19A=
NM_001258332.2:c.493+19A=	NP_001245261.1:n.493+19A=