Canonical Allele Identifier: CA416614953

Gene: GALE

Linked Data

• MyVariant Identifiers: chr1:g.24123053T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23796563T>A , CM000663.2:g.23796563T>A	GRCh38
NC_000001.10:g.24123053T>A , CM000663.1:g.24123053T>A	GRCh37
NC_000001.9:g.23995640T>A	NCBI36
NG_007068.1:g.9242A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.819A>T MANE Select	ENSP00000483375.1:p.Thr273=
ENST00000374497.7:c.819A>T	ENSP00000363621.3:p.Thr273=
ENST00000418277.5:c.627A>T	ENSP00000414719.1:p.Thr209=
ENST00000429356.5:c.603+134A>T	ENSP00000398585.1:n.603+134A>T
ENST00000456977.5:c.153+134A>T	ENSP00000397045.1:n.153+134A>T
ENST00000459934.5:n.1047A>T
ENST00000469556.1:n.323A>T
ENST00000481736.5:n.1223A>T
ENST00000617979.4:c.819A>T	ENSP00000483375.1:p.Thr273=
NM_000403.3:c.819A>T	NP_000394.2:p.Thr273=
NM_001008216.1:c.819A>T	NP_001008217.1:p.Thr273=
NM_001127621.1:c.819A>T	NP_001121093.1:p.Thr273=
NM_001008216.2:c.819A>T MANE Select	NP_001008217.1:p.Thr273=
NM_000403.4:c.819A>T	NP_000394.2:p.Thr273=
NM_001127621.2:c.819A>T	NP_001121093.1:p.Thr273=