Canonical Allele Identifier: CA1845636035

Gene: GALT

Linked Data

• dbSNP Id: rs1564100884

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647431A>G , CM000671.2:g.34647431A>G	GRCh38
NC_000009.11:g.34647428A>G , CM000671.1:g.34647428A>G	GRCh37
NC_000009.10:g.34637428A>G	NCBI36
NG_009029.1:g.5794A>G
NG_028966.1:g.247A>G
NG_009029.2:g.5843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.253-61A>G	ENSP00000509954.1:n.253-61A>G
ENST00000378842.8:c.253-61A>G MANE Select	ENSP00000368119.4:n.253-61A>G
ENST00000378842.7:c.253-61A>G	ENSP00000368119.3:n.253-61A>G
ENST00000450095.6:c.50+173A>G	ENSP00000401956.2:n.50+173A>G
ENST00000465543.6:n.592-61A>G
ENST00000468099.2:n.465A>G
ENST00000472111.5:n.294-61A>G
ENST00000473506.6:c.253-110A>G	ENSP00000432839.2:n.253-110A>G
ENST00000473529.5:n.300-61A>G
ENST00000485531.1:n.418A>G
ENST00000487381.5:n.451A>G
ENST00000489643.6:n.282+173A>G
ENST00000554085.5:c.253-44A>G	ENSP00000450419.1:n.253-44A>G
ENST00000554139.5:n.306-61A>G
ENST00000554330.5:n.250-110A>G
ENST00000554550.5:c.252+173A>G	ENSP00000451435.1:n.252+173A>G
ENST00000554638.5:n.449A>G
ENST00000554897.5:c.252+173A>G	ENSP00000450942.1:n.252+173A>G
ENST00000554944.5:n.283-110A>G
ENST00000555020.5:n.283-61A>G
ENST00000555086.5:n.257-61A>G
ENST00000555214.5:n.261+173A>G
ENST00000556157.1:n.360-44A>G
ENST00000556244.1:c.179A>G
ENST00000556278.1:c.252+173A>G	ENSP00000451792.1:n.252+173A>G
ENST00000556403.5:n.266-61A>G
ENST00000556494.5:n.285-61A>G
ENST00000557541.5:n.446-110A>G
ENST00000557706.5:n.539A>G
NM_000155.3:c.253-61A>G	NP_000146.2:n.253-61A>G
NM_001258332.1:c.50+173A>G	NP_001245261.1:n.50+173A>G
NM_000155.4:c.253-61A>G MANE Select	NP_000146.2:n.253-61A>G
NM_001258332.2:c.50+173A>G	NP_001245261.1:n.50+173A>G