Canonical Allele Identifier: CA2579371145

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647396C>A , CM000671.2:g.34647396C>A	GRCh38
NC_000009.11:g.34647393C>A , CM000671.1:g.34647393C>A	GRCh37
NC_000009.10:g.34637393C>A	NCBI36
NG_009029.1:g.5759C>A
NG_028966.1:g.212C>A
NG_009029.2:g.5808C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.253-96C>A	ENSP00000509954.1:n.253-96C>A
ENST00000378842.8:c.253-96C>A MANE Select	ENSP00000368119.4:n.253-96C>A
ENST00000378842.7:c.253-96C>A	ENSP00000368119.3:n.253-96C>A
ENST00000450095.6:c.50+138C>A	ENSP00000401956.2:n.50+138C>A
ENST00000465543.6:n.592-96C>A
ENST00000468099.2:n.430C>A
ENST00000472111.5:n.294-96C>A
ENST00000473506.6:c.252+138C>A	ENSP00000432839.2:n.252+138C>A
ENST00000473529.5:n.300-96C>A
ENST00000485531.1:n.383C>A
ENST00000487381.5:n.416C>A
ENST00000489643.6:n.282+138C>A
ENST00000554085.5:c.253-79C>A	ENSP00000450419.1:n.253-79C>A
ENST00000554139.5:n.306-96C>A
ENST00000554330.5:n.249+138C>A
ENST00000554550.5:c.252+138C>A	ENSP00000451435.1:n.252+138C>A
ENST00000554638.5:n.414C>A
ENST00000554897.5:c.252+138C>A	ENSP00000450942.1:n.252+138C>A
ENST00000554944.5:n.282+138C>A
ENST00000555020.5:n.283-96C>A
ENST00000555086.5:n.257-96C>A
ENST00000555214.5:n.261+138C>A
ENST00000556157.1:n.360-79C>A
ENST00000556244.1:c.144C>A
ENST00000556278.1:c.252+138C>A	ENSP00000451792.1:n.252+138C>A
ENST00000556403.5:n.266-96C>A
ENST00000556494.5:n.285-96C>A
ENST00000557541.5:n.445+138C>A
ENST00000557706.5:n.504C>A
NM_000155.3:c.253-96C>A	NP_000146.2:n.253-96C>A
NM_001258332.1:c.50+138C>A	NP_001245261.1:n.50+138C>A
NM_000155.4:c.253-96C>A MANE Select	NP_000146.2:n.253-96C>A
NM_001258332.2:c.50+138C>A	NP_001245261.1:n.50+138C>A