Canonical Allele Identifier: CA2689808611

Gene: GALT

Linked Data

• gnomAD v4: 9-34647444-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647444A>T , CM000671.2:g.34647444A>T	GRCh38
NC_000009.11:g.34647441A>T , CM000671.1:g.34647441A>T	GRCh37
NC_000009.10:g.34637441A>T	NCBI36
NG_009029.1:g.5807A>T
NG_028966.1:g.260A>T
NG_009029.2:g.5856A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.253-48A>T	ENSP00000509954.1:n.253-48A>T
ENST00000378842.8:c.253-48A>T MANE Select	ENSP00000368119.4:n.253-48A>T
ENST00000378842.7:c.253-48A>T	ENSP00000368119.3:n.253-48A>T
ENST00000450095.6:c.50+186A>T	ENSP00000401956.2:n.50+186A>T
ENST00000465543.6:n.592-48A>T
ENST00000468099.2:n.478A>T
ENST00000472111.5:n.294-48A>T
ENST00000473506.6:c.253-97A>T	ENSP00000432839.2:n.253-97A>T
ENST00000473529.5:n.300-48A>T
ENST00000485531.1:n.431A>T
ENST00000487381.5:n.464A>T
ENST00000489643.6:n.282+186A>T
ENST00000554085.5:c.253-31A>T	ENSP00000450419.1:n.253-31A>T
ENST00000554139.5:n.306-48A>T
ENST00000554330.5:n.250-97A>T
ENST00000554550.5:c.252+186A>T	ENSP00000451435.1:n.252+186A>T
ENST00000554638.5:n.462A>T
ENST00000554897.5:c.252+186A>T	ENSP00000450942.1:n.252+186A>T
ENST00000554944.5:n.283-97A>T
ENST00000555020.5:n.283-48A>T
ENST00000555086.5:n.257-48A>T
ENST00000555214.5:n.261+186A>T
ENST00000556157.1:n.360-31A>T
ENST00000556244.1:c.192A>T
ENST00000556278.1:c.252+186A>T	ENSP00000451792.1:n.252+186A>T
ENST00000556403.5:n.266-48A>T
ENST00000556494.5:n.285-48A>T
ENST00000557541.5:n.446-97A>T
ENST00000557706.5:n.552A>T
NM_000155.3:c.253-48A>T	NP_000146.2:n.253-48A>T
NM_001258332.1:c.50+186A>T	NP_001245261.1:n.50+186A>T
NM_000155.4:c.253-48A>T MANE Select	NP_000146.2:n.253-48A>T
NM_001258332.2:c.50+186A>T	NP_001245261.1:n.50+186A>T