Canonical Allele Identifier: CA464595668

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647114G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647117G>C , CM000671.2:g.34647117G>C	GRCh38
NC_000009.11:g.34647114G>C , CM000671.1:g.34647114G>C	GRCh37
NC_000009.10:g.34637114G>C	NCBI36
NG_009029.1:g.5480G>C
NG_009029.2:g.5529G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.111G>C	ENSP00000509954.1:p.Leu37=
ENST00000378842.8:c.111G>C MANE Select	ENSP00000368119.4:p.Leu37=
ENST00000378842.7:c.111G>C	ENSP00000368119.3:p.Leu37=
ENST00000450095.6:c.-92G>C	ENSP00000401956.2:n.-92G>C
ENST00000465543.6:n.450G>C
ENST00000468099.2:n.155-4G>C
ENST00000472111.5:n.152G>C
ENST00000473506.6:c.111G>C	ENSP00000432839.2:p.Leu37=
ENST00000473529.5:n.158G>C
ENST00000485531.1:n.104G>C
ENST00000487381.5:n.137G>C
ENST00000489643.6:n.141G>C
ENST00000554085.5:c.111G>C	ENSP00000450419.1:p.Leu37=
ENST00000554139.5:n.164G>C
ENST00000554330.5:n.108G>C
ENST00000554550.5:c.111G>C	ENSP00000451435.1:p.Leu37=
ENST00000554638.5:n.135G>C
ENST00000554897.5:c.111G>C	ENSP00000450942.1:p.Leu37=
ENST00000554944.5:n.141G>C
ENST00000555020.5:n.141G>C
ENST00000555086.5:n.115G>C
ENST00000555214.5:n.120G>C
ENST00000556157.1:n.218G>C
ENST00000556278.1:c.111G>C	ENSP00000451792.1:p.Leu37=
ENST00000556403.5:n.124G>C
ENST00000556494.5:n.143G>C
ENST00000557541.5:n.304G>C
ENST00000557706.5:n.225G>C
ENST00000605275.1:n.649G>C
NM_000155.3:c.111G>C	NP_000146.2:p.Leu37=
NM_001258332.1:c.-92G>C	NP_001245261.1:n.-92G>C
NM_000155.4:c.111G>C MANE Select	NP_000146.2:p.Leu37=
NM_001258332.2:c.-92G>C	NP_001245261.1:n.-92G>C