Canonical Allele Identifier: CA373278162

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34646704G>C (hg19) ; chr9:g.34646707G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646707G>C , CM000671.2:g.34646707G>C	GRCh38
NC_000009.11:g.34646704G>C , CM000671.1:g.34646704G>C	GRCh37
NC_000009.10:g.34636704G>C	NCBI36
NG_009029.1:g.5070G>C
NG_009029.2:g.5119G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.3G>C	ENSP00000509954.1:p.Met1Ile
ENST00000378842.8:c.3G>C MANE Select	ENSP00000368119.4:p.Met1Ile
ENST00000378842.7:c.3G>C	ENSP00000368119.3:p.Met1Ile
ENST00000450095.6:c.-200G>C	ENSP00000401956.2:n.-200G>C
ENST00000465543.6:n.40G>C
ENST00000468099.2:n.75G>C
ENST00000472111.5:n.44G>C
ENST00000473506.6:c.3G>C	ENSP00000432839.2:p.Met1Ile
ENST00000473529.5:n.50G>C
ENST00000487381.5:n.29G>C
ENST00000489643.6:n.33G>C
ENST00000554085.5:c.3G>C	ENSP00000450419.1:p.Met1Ile
ENST00000554139.5:n.56G>C
ENST00000554550.5:c.3G>C	ENSP00000451435.1:p.Met1Ile
ENST00000554638.5:n.27G>C
ENST00000554897.5:c.3G>C	ENSP00000450942.1:p.Met1Ile
ENST00000554944.5:n.33G>C
ENST00000555020.5:n.33G>C
ENST00000555214.5:n.12G>C
ENST00000556278.1:c.3G>C	ENSP00000451792.1:p.Met1Ile
ENST00000557541.5:n.63G>C
ENST00000605275.1:n.239G>C
NM_000155.3:c.3G>C	NP_000146.2:p.Met1Ile
NM_001258332.1:c.-200G>C	NP_001245261.1:n.-200G>C
NM_000155.4:c.3G>C MANE Select	NP_000146.2:p.Met1Ile
NM_001258332.2:c.-200G>C	NP_001245261.1:n.-200G>C