Canonical Allele Identifier: CA339006861

Gene: GALE

Linked Data

• MyVariant Identifiers: chr1:g.24123071G>T (hg19) ; chr1:g.23796581G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23796581G>T , CM000663.2:g.23796581G>T	GRCh38
NC_000001.10:g.24123071G>T , CM000663.1:g.24123071G>T	GRCh37
NC_000001.9:g.23995658G>T	NCBI36
NG_007068.1:g.9224C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.801C>A MANE Select	ENSP00000483375.1:p.Tyr267Ter
ENST00000374497.7:c.801C>A	ENSP00000363621.3:p.Tyr267Ter
ENST00000418277.5:c.609C>A	ENSP00000414719.1:p.Tyr203Ter
ENST00000429356.5:c.603+116C>A	ENSP00000398585.1:n.603+116C>A
ENST00000456977.5:c.153+116C>A	ENSP00000397045.1:n.153+116C>A
ENST00000459934.5:n.1029C>A
ENST00000469556.1:n.305C>A
ENST00000481736.5:n.1205C>A
ENST00000617979.4:c.801C>A	ENSP00000483375.1:p.Tyr267Ter
NM_000403.3:c.801C>A	NP_000394.2:p.Tyr267Ter
NM_001008216.1:c.801C>A	NP_001008217.1:p.Tyr267Ter
NM_001127621.1:c.801C>A	NP_001121093.1:p.Tyr267Ter
NM_001008216.2:c.801C>A MANE Select	NP_001008217.1:p.Tyr267Ter
NM_000403.4:c.801C>A	NP_000394.2:p.Tyr267Ter
NM_001127621.2:c.801C>A	NP_001121093.1:p.Tyr267Ter