Canonical Allele Identifier: CA373278566

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647125G>C (hg19) ; chr9:g.34647128G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647128G>C , CM000671.2:g.34647128G>C	GRCh38
NC_000009.11:g.34647125G>C , CM000671.1:g.34647125G>C	GRCh37
NC_000009.10:g.34637125G>C	NCBI36
NG_009029.1:g.5491G>C
NG_009029.2:g.5540G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.122G>C	ENSP00000509954.1:p.Trp41Ser
ENST00000378842.8:c.122G>C MANE Select	ENSP00000368119.4:p.Trp41Ser
ENST00000378842.7:c.122G>C	ENSP00000368119.3:p.Trp41Ser
ENST00000450095.6:c.-81G>C	ENSP00000401956.2:n.-81G>C
ENST00000465543.6:n.461G>C
ENST00000468099.2:n.162G>C
ENST00000472111.5:n.163G>C
ENST00000473506.6:c.122G>C	ENSP00000432839.2:p.Trp41Ser
ENST00000473529.5:n.169G>C
ENST00000485531.1:n.115G>C
ENST00000487381.5:n.148G>C
ENST00000489643.6:n.152G>C
ENST00000554085.5:c.122G>C	ENSP00000450419.1:p.Trp41Ser
ENST00000554139.5:n.175G>C
ENST00000554330.5:n.119G>C
ENST00000554550.5:c.122G>C	ENSP00000451435.1:p.Trp41Ser
ENST00000554638.5:n.146G>C
ENST00000554897.5:c.122G>C	ENSP00000450942.1:p.Trp41Ser
ENST00000554944.5:n.152G>C
ENST00000555020.5:n.152G>C
ENST00000555086.5:n.126G>C
ENST00000555214.5:n.131G>C
ENST00000556157.1:n.229G>C
ENST00000556244.1:c.6G>C
ENST00000556278.1:c.122G>C	ENSP00000451792.1:p.Trp41Ser
ENST00000556403.5:n.135G>C
ENST00000556494.5:n.154G>C
ENST00000557541.5:n.315G>C
ENST00000557706.5:n.236G>C
ENST00000605275.1:n.660G>C
NM_000155.3:c.122G>C	NP_000146.2:p.Trp41Ser
NM_001258332.1:c.-81G>C	NP_001245261.1:n.-81G>C
NM_000155.4:c.122G>C MANE Select	NP_000146.2:p.Trp41Ser
NM_001258332.2:c.-81G>C	NP_001245261.1:n.-81G>C