Canonical Allele Identifier: CA1158961406

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798151_23798153delinsCTG , CM000663.2:g.23798151_23798153delinsCTG	GRCh38
NC_000001.10:g.24124641_24124643delinsCTG , CM000663.1:g.24124641_24124643delinsCTG	GRCh37
NC_000001.9:g.23997228_23997230delinsCTG	NCBI36
NG_007068.1:g.7652_7654delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.315_317delinsCAG MANE Select	ENSP00000483375.1:p.Tyr105=
ENST00000374497.7:c.315_317delinsCAG	ENSP00000363621.3:p.Tyr105=
ENST00000418277.5:c.123_125delinsCAG	ENSP00000414719.1:p.Tyr41=
ENST00000425913.5:c.315_317delinsCAG	ENSP00000393359.1:p.Tyr105=
ENST00000429356.5:c.123_125delinsCAG	ENSP00000398585.1:p.Tyr41=
ENST00000445705.1:c.315_317delinsCAG	ENSP00000398257.1:p.Tyr105=
ENST00000459934.5:n.433_435delinsCAG
ENST00000467493.5:n.775_777delinsCAG
ENST00000470949.5:n.260_262delinsCAG
ENST00000481736.5:n.719_721delinsCAG
ENST00000486382.1:n.416_418delinsCAG
ENST00000617979.4:c.315_317delinsCAG	ENSP00000483375.1:p.Tyr105=
NM_000403.3:c.315_317delinsCAG	NP_000394.2:p.Tyr105=
NM_001008216.1:c.315_317delinsCAG	NP_001008217.1:p.Tyr105=
NM_001127621.1:c.315_317delinsCAG	NP_001121093.1:p.Tyr105=
NM_001008216.2:c.315_317delinsCAG MANE Select	NP_001008217.1:p.Tyr105=
NM_000403.4:c.315_317delinsCAG	NP_000394.2:p.Tyr105=
NM_001127621.2:c.315_317delinsCAG	NP_001121093.1:p.Tyr105=