Canonical Allele Identifier: CA1158961356

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798038_23798040delinsCTG , CM000663.2:g.23798038_23798040delinsCTG	GRCh38
NC_000001.10:g.24124528_24124530delinsCTG , CM000663.1:g.24124528_24124530delinsCTG	GRCh37
NC_000001.9:g.23997115_23997117delinsCTG	NCBI36
NG_007068.1:g.7765_7767delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.351+77_351+79delinsCAG MANE Select	ENSP00000483375.1:n.351+77_351+79delinsCAG
ENST00000374497.7:c.351+77_351+79delinsCAG	ENSP00000363621.3:n.351+77_351+79delinsCAG
ENST00000418277.5:c.159+77_159+79delinsCAG	ENSP00000414719.1:n.159+77_159+79delinsCAG
ENST00000425913.5:c.351+77_351+79delinsCAG	ENSP00000393359.1:n.351+77_351+79delinsCAG
ENST00000429356.5:c.159+77_159+79delinsCAG	ENSP00000398585.1:n.159+77_159+79delinsCAG
ENST00000445705.1:c.351+77_351+79delinsCAG	ENSP00000398257.1:n.351+77_351+79delinsCAG
ENST00000459934.5:n.469+77_469+79delinsCAG
ENST00000467493.5:n.811+77_811+79delinsCAG
ENST00000470949.5:n.296+77_296+79delinsCAG
ENST00000481736.5:n.755+77_755+79delinsCAG
ENST00000617979.4:c.351+77_351+79delinsCAG	ENSP00000483375.1:n.351+77_351+79delinsCAG
NM_000403.3:c.351+77_351+79delinsCAG	NP_000394.2:n.351+77_351+79delinsCAG
NM_001008216.1:c.351+77_351+79delinsCAG	NP_001008217.1:n.351+77_351+79delinsCAG
NM_001127621.1:c.351+77_351+79delinsCAG	NP_001121093.1:n.351+77_351+79delinsCAG
NM_001008216.2:c.351+77_351+79delinsCAG MANE Select	NP_001008217.1:n.351+77_351+79delinsCAG
NM_000403.4:c.351+77_351+79delinsCAG	NP_000394.2:n.351+77_351+79delinsCAG
NM_001127621.2:c.351+77_351+79delinsCAG	NP_001121093.1:n.351+77_351+79delinsCAG