Canonical Allele Identifier: CA2689808603

Gene: GALT

Linked Data

• gnomAD v4: 9-34647408-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647408C>T , CM000671.2:g.34647408C>T	GRCh38
NC_000009.11:g.34647405C>T , CM000671.1:g.34647405C>T	GRCh37
NC_000009.10:g.34637405C>T	NCBI36
NG_009029.1:g.5771C>T
NG_028966.1:g.224C>T
NG_009029.2:g.5820C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.253-84C>T	ENSP00000509954.1:n.253-84C>T
ENST00000378842.8:c.253-84C>T MANE Select	ENSP00000368119.4:n.253-84C>T
ENST00000378842.7:c.253-84C>T	ENSP00000368119.3:n.253-84C>T
ENST00000450095.6:c.50+150C>T	ENSP00000401956.2:n.50+150C>T
ENST00000465543.6:n.592-84C>T
ENST00000468099.2:n.442C>T
ENST00000472111.5:n.294-84C>T
ENST00000473506.6:c.253-133C>T	ENSP00000432839.2:n.253-133C>T
ENST00000473529.5:n.300-84C>T
ENST00000485531.1:n.395C>T
ENST00000487381.5:n.428C>T
ENST00000489643.6:n.282+150C>T
ENST00000554085.5:c.253-67C>T	ENSP00000450419.1:n.253-67C>T
ENST00000554139.5:n.306-84C>T
ENST00000554330.5:n.250-133C>T
ENST00000554550.5:c.252+150C>T	ENSP00000451435.1:n.252+150C>T
ENST00000554638.5:n.426C>T
ENST00000554897.5:c.252+150C>T	ENSP00000450942.1:n.252+150C>T
ENST00000554944.5:n.283-133C>T
ENST00000555020.5:n.283-84C>T
ENST00000555086.5:n.257-84C>T
ENST00000555214.5:n.261+150C>T
ENST00000556157.1:n.360-67C>T
ENST00000556244.1:c.156C>T
ENST00000556278.1:c.252+150C>T	ENSP00000451792.1:n.252+150C>T
ENST00000556403.5:n.266-84C>T
ENST00000556494.5:n.285-84C>T
ENST00000557541.5:n.446-133C>T
ENST00000557706.5:n.516C>T
NM_000155.3:c.253-84C>T	NP_000146.2:n.253-84C>T
NM_001258332.1:c.50+150C>T	NP_001245261.1:n.50+150C>T
NM_000155.4:c.253-84C>T MANE Select	NP_000146.2:n.253-84C>T
NM_001258332.2:c.50+150C>T	NP_001245261.1:n.50+150C>T