Canonical Allele Identifier: CA464403022

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648803C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648806C>G , CM000671.2:g.34648806C>G	GRCh38
NC_000009.11:g.34648803C>G , CM000671.1:g.34648803C>G	GRCh37
NC_000009.10:g.34638803C>G	NCBI36
NG_009029.1:g.7169C>G
NG_028966.1:g.1622C>G
NG_009029.2:g.7218C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*320C>G	ENSP00000509954.1:n.*320C>G
ENST00000378842.8:c.732C>G MANE Select	ENSP00000368119.4:p.Pro244=
ENST00000378842.7:c.732C>G	ENSP00000368119.3:p.Pro244=
ENST00000450095.6:c.405C>G	ENSP00000401956.2:p.Pro135=
ENST00000473506.6:c.*320C>G	ENSP00000432839.2:n.*320C>G
ENST00000473529.5:n.891C>G
ENST00000487381.5:n.1422C>G
ENST00000489643.6:n.812C>G
ENST00000554085.5:c.*476C>G	ENSP00000450419.1:n.*476C>G
ENST00000554550.5:c.*352C>G	ENSP00000451435.1:n.*352C>G
ENST00000554638.5:n.1204C>G
ENST00000555020.5:n.1193C>G
ENST00000555086.5:n.736C>G
ENST00000555754.1:n.77C>G
ENST00000556244.1:c.719C>G
ENST00000556278.1:c.432+350C>G	ENSP00000451792.1:n.432+350C>G
ENST00000557706.5:n.1294C>G
NM_000155.3:c.732C>G	NP_000146.2:p.Pro244=
NM_001258332.1:c.405C>G	NP_001245261.1:p.Pro135=
NM_000155.4:c.732C>G MANE Select	NP_000146.2:p.Pro244=
NM_001258332.2:c.405C>G	NP_001245261.1:p.Pro135=