Canonical Allele Identifier: CA464595848

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647688T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647691T>A , CM000671.2:g.34647691T>A	GRCh38
NC_000009.11:g.34647688T>A , CM000671.1:g.34647688T>A	GRCh37
NC_000009.10:g.34637688T>A	NCBI36
NG_009029.1:g.6054T>A
NG_028966.1:g.507T>A
NG_009029.2:g.6103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+124T>A	ENSP00000509954.1:n.328+124T>A
ENST00000378842.8:c.363T>A MANE Select	ENSP00000368119.4:p.Ser121=
ENST00000378842.7:c.363T>A	ENSP00000368119.3:p.Ser121=
ENST00000450095.6:c.51-141T>A	ENSP00000401956.2:n.51-141T>A
ENST00000465543.6:n.702T>A
ENST00000472111.5:n.493T>A
ENST00000473506.6:c.314T>A	ENSP00000432839.2:p.Leu105Gln
ENST00000473529.5:n.499T>A
ENST00000485531.1:n.678T>A
ENST00000487381.5:n.622T>A
ENST00000489643.6:n.283-424T>A
ENST00000554085.5:c.*107T>A	ENSP00000450419.1:n.*107T>A
ENST00000554139.5:n.416T>A
ENST00000554330.5:n.400T>A
ENST00000554550.5:c.253-141T>A	ENSP00000451435.1:n.253-141T>A
ENST00000554638.5:n.709T>A
ENST00000554897.5:c.253-141T>A	ENSP00000450942.1:n.253-141T>A
ENST00000554944.5:n.433T>A
ENST00000555020.5:n.393T>A
ENST00000555086.5:n.367T>A
ENST00000555214.5:n.262-357T>A
ENST00000556157.1:n.487T>A
ENST00000556244.1:c.350T>A
ENST00000556278.1:c.253-424T>A	ENSP00000451792.1:n.253-424T>A
ENST00000556403.5:n.465T>A
ENST00000556494.5:n.484T>A
ENST00000557541.5:n.507T>A
ENST00000557706.5:n.799T>A
NM_000155.3:c.363T>A	NP_000146.2:p.Ser121=
NM_001258332.1:c.51-141T>A	NP_001245261.1:n.51-141T>A
NM_000155.4:c.363T>A MANE Select	NP_000146.2:p.Ser121=
NM_001258332.2:c.51-141T>A	NP_001245261.1:n.51-141T>A