Canonical Allele Identifier: CA1845638954

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648425T= , CM000671.2:g.34648425T=	GRCh38
NC_000009.11:g.34648422T= , CM000671.1:g.34648422T=	GRCh37
NC_000009.10:g.34638422T=	NCBI36
NG_009029.1:g.6788T=
NG_028966.1:g.1241T=
NG_009029.2:g.6837T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*244T=	ENSP00000509954.1:n.*244T=
ENST00000378842.8:c.656T= MANE Select	ENSP00000368119.4:p.Met219=
ENST00000378842.7:c.656T=	ENSP00000368119.3:p.Met219=
ENST00000450095.6:c.329T=	ENSP00000401956.2:p.Met110=
ENST00000472111.5:n.912T=
ENST00000473506.6:c.*244T=	ENSP00000432839.2:n.*244T=
ENST00000473529.5:n.815T=
ENST00000487381.5:n.1041T=
ENST00000489643.6:n.431T=
ENST00000554085.5:c.*400T=	ENSP00000450419.1:n.*400T=
ENST00000554550.5:c.*276T=	ENSP00000451435.1:n.*276T=
ENST00000554638.5:n.1128T=
ENST00000555020.5:n.812T=
ENST00000555086.5:n.660T=
ENST00000555214.5:n.477T=
ENST00000555754.1:n.1T=
ENST00000556244.1:c.643T=
ENST00000556278.1:c.401T=	ENSP00000451792.1:p.Met134=
ENST00000556494.5:n.777T=
ENST00000557706.5:n.1218T=
NM_000155.3:c.656T=	NP_000146.2:p.Met219=
NM_001258332.1:c.329T=	NP_001245261.1:p.Met110=
NM_000155.4:c.656T= MANE Select	NP_000146.2:p.Met219=
NM_001258332.2:c.329T=	NP_001245261.1:p.Met110=