Canonical Allele Identifier: CA464403225

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648857G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648860G>C , CM000671.2:g.34648860G>C	GRCh38
NC_000009.11:g.34648857G>C , CM000671.1:g.34648857G>C	GRCh37
NC_000009.10:g.34638857G>C	NCBI36
NG_009029.1:g.7223G>C
NG_028966.1:g.1676G>C
NG_009029.2:g.7272G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*374G>C	ENSP00000509954.1:n.*374G>C
ENST00000378842.8:c.786G>C MANE Select	ENSP00000368119.4:p.Arg262=
ENST00000378842.7:c.786G>C	ENSP00000368119.3:p.Arg262=
ENST00000450095.6:c.459G>C	ENSP00000401956.2:p.Arg153=
ENST00000473506.6:c.*374G>C	ENSP00000432839.2:n.*374G>C
ENST00000489643.6:n.866G>C
ENST00000554085.5:c.*530G>C	ENSP00000450419.1:n.*530G>C
ENST00000554550.5:c.*406G>C	ENSP00000451435.1:n.*406G>C
ENST00000554638.5:n.1258G>C
ENST00000555020.5:n.1247G>C
ENST00000555086.5:n.790G>C
ENST00000555754.1:n.131G>C
ENST00000556244.1:c.773G>C
ENST00000556278.1:c.432+404G>C	ENSP00000451792.1:n.432+404G>C
ENST00000557706.5:n.1348G>C
NM_000155.3:c.786G>C	NP_000146.2:p.Arg262=
NM_001258332.1:c.459G>C	NP_001245261.1:p.Arg153=
NM_000155.4:c.786G>C MANE Select	NP_000146.2:p.Arg262=
NM_001258332.2:c.459G>C	NP_001245261.1:p.Arg153=