Canonical Allele Identifier: CA373278498

Gene: GALT

Linked Data

• gnomAD v4: 9-34647101-T-C
• MyVariant Identifiers: chr9:g.34647098T>C (hg19) ; chr9:g.34647101T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647101T>C , CM000671.2:g.34647101T>C	GRCh38
NC_000009.11:g.34647098T>C , CM000671.1:g.34647098T>C	GRCh37
NC_000009.10:g.34637098T>C	NCBI36
NG_009029.1:g.5464T>C
NG_009029.2:g.5513T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.95T>C	ENSP00000509954.1:p.Ile32Thr
ENST00000378842.8:c.95T>C MANE Select	ENSP00000368119.4:p.Ile32Thr
ENST00000378842.7:c.95T>C	ENSP00000368119.3:p.Ile32Thr
ENST00000450095.6:c.-108T>C	ENSP00000401956.2:n.-108T>C
ENST00000465543.6:n.434T>C
ENST00000468099.2:n.155-20T>C
ENST00000472111.5:n.136T>C
ENST00000473506.6:c.95T>C	ENSP00000432839.2:p.Ile32Thr
ENST00000473529.5:n.142T>C
ENST00000485531.1:n.88T>C
ENST00000487381.5:n.121T>C
ENST00000489643.6:n.125T>C
ENST00000554085.5:c.95T>C	ENSP00000450419.1:p.Ile32Thr
ENST00000554139.5:n.148T>C
ENST00000554330.5:n.92T>C
ENST00000554550.5:c.95T>C	ENSP00000451435.1:p.Ile32Thr
ENST00000554638.5:n.119T>C
ENST00000554897.5:c.95T>C	ENSP00000450942.1:p.Ile32Thr
ENST00000554944.5:n.125T>C
ENST00000555020.5:n.125T>C
ENST00000555086.5:n.99T>C
ENST00000555214.5:n.104T>C
ENST00000556157.1:n.202T>C
ENST00000556278.1:c.95T>C	ENSP00000451792.1:p.Ile32Thr
ENST00000556403.5:n.108T>C
ENST00000556494.5:n.127T>C
ENST00000557541.5:n.288T>C
ENST00000557706.5:n.209T>C
ENST00000605275.1:n.633T>C
NM_000155.3:c.95T>C	NP_000146.2:p.Ile32Thr
NM_001258332.1:c.-108T>C	NP_001245261.1:n.-108T>C
NM_000155.4:c.95T>C MANE Select	NP_000146.2:p.Ile32Thr
NM_001258332.2:c.-108T>C	NP_001245261.1:n.-108T>C