Canonical Allele Identifier: CA464595753

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647563A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647566A>C , CM000671.2:g.34647566A>C	GRCh38
NC_000009.11:g.34647563A>C , CM000671.1:g.34647563A>C	GRCh37
NC_000009.10:g.34637563A>C	NCBI36
NG_009029.1:g.5929A>C
NG_028966.1:g.382A>C
NG_009029.2:g.5978A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.327A>C	ENSP00000509954.1:p.Pro109=
ENST00000378842.8:c.327A>C MANE Select	ENSP00000368119.4:p.Pro109=
ENST00000378842.7:c.327A>C	ENSP00000368119.3:p.Pro109=
ENST00000450095.6:c.51-266A>C	ENSP00000401956.2:n.51-266A>C
ENST00000465543.6:n.666A>C
ENST00000472111.5:n.368A>C
ENST00000473506.6:c.278A>C	ENSP00000432839.2:p.Gln93Pro
ENST00000473529.5:n.374A>C
ENST00000485531.1:n.553A>C
ENST00000487381.5:n.586A>C
ENST00000489643.6:n.282+308A>C
ENST00000554085.5:c.*71A>C	ENSP00000450419.1:n.*71A>C
ENST00000554139.5:n.380A>C
ENST00000554330.5:n.275A>C
ENST00000554550.5:c.253-266A>C	ENSP00000451435.1:n.253-266A>C
ENST00000554638.5:n.584A>C
ENST00000554897.5:c.253-266A>C	ENSP00000450942.1:n.253-266A>C
ENST00000554944.5:n.308A>C
ENST00000555020.5:n.357A>C
ENST00000555086.5:n.331A>C
ENST00000555214.5:n.261+308A>C
ENST00000556157.1:n.451A>C
ENST00000556244.1:c.314A>C
ENST00000556278.1:c.252+308A>C	ENSP00000451792.1:n.252+308A>C
ENST00000556403.5:n.340A>C
ENST00000556494.5:n.359A>C
ENST00000557541.5:n.471A>C
ENST00000557706.5:n.674A>C
NM_000155.3:c.327A>C	NP_000146.2:p.Pro109=
NM_001258332.1:c.51-266A>C	NP_001245261.1:n.51-266A>C
NM_000155.4:c.327A>C MANE Select	NP_000146.2:p.Pro109=
NM_001258332.2:c.51-266A>C	NP_001245261.1:n.51-266A>C