Canonical Allele Identifier: CA2783504171

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647399C>T , CM000671.2:g.34647399C>T	GRCh38
NC_000009.11:g.34647396C>T , CM000671.1:g.34647396C>T	GRCh37
NC_000009.10:g.34637396C>T	NCBI36
NG_009029.1:g.5762C>T
NG_028966.1:g.215C>T
NG_009029.2:g.5811C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.253-93C>T	ENSP00000509954.1:n.253-93C>T
ENST00000378842.8:c.253-93C>T MANE Select	ENSP00000368119.4:n.253-93C>T
ENST00000378842.7:c.253-93C>T	ENSP00000368119.3:n.253-93C>T
ENST00000450095.6:c.50+141C>T	ENSP00000401956.2:n.50+141C>T
ENST00000465543.6:n.592-93C>T
ENST00000468099.2:n.433C>T
ENST00000472111.5:n.294-93C>T
ENST00000473506.6:c.253-142C>T	ENSP00000432839.2:n.253-142C>T
ENST00000473529.5:n.300-93C>T
ENST00000485531.1:n.386C>T
ENST00000487381.5:n.419C>T
ENST00000489643.6:n.282+141C>T
ENST00000554085.5:c.253-76C>T	ENSP00000450419.1:n.253-76C>T
ENST00000554139.5:n.306-93C>T
ENST00000554330.5:n.250-142C>T
ENST00000554550.5:c.252+141C>T	ENSP00000451435.1:n.252+141C>T
ENST00000554638.5:n.417C>T
ENST00000554897.5:c.252+141C>T	ENSP00000450942.1:n.252+141C>T
ENST00000554944.5:n.283-142C>T
ENST00000555020.5:n.283-93C>T
ENST00000555086.5:n.257-93C>T
ENST00000555214.5:n.261+141C>T
ENST00000556157.1:n.360-76C>T
ENST00000556244.1:c.147C>T
ENST00000556278.1:c.252+141C>T	ENSP00000451792.1:n.252+141C>T
ENST00000556403.5:n.266-93C>T
ENST00000556494.5:n.285-93C>T
ENST00000557541.5:n.446-142C>T
ENST00000557706.5:n.507C>T
NM_000155.3:c.253-93C>T	NP_000146.2:n.253-93C>T
NM_001258332.1:c.50+141C>T	NP_001245261.1:n.50+141C>T
NM_000155.4:c.253-93C>T MANE Select	NP_000146.2:n.253-93C>T
NM_001258332.2:c.50+141C>T	NP_001245261.1:n.50+141C>T