Canonical Allele Identifier: CA1158961429

Gene: GALE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798203_23798204delinsCA , CM000663.2:g.23798203_23798204delinsCA	GRCh38
NC_000001.10:g.24124693_24124694delinsCA , CM000663.1:g.24124693_24124694delinsCA	GRCh37
NC_000001.9:g.23997280_23997281delinsCA	NCBI36
NG_007068.1:g.7601_7602delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.264_265delinsTG MANE Select	ENSP00000483375.1:p.Phe88=
ENST00000374497.7:c.264_265delinsTG	ENSP00000363621.3:p.Phe88=
ENST00000418277.5:c.72_73delinsTG	ENSP00000414719.1:p.Phe24=
ENST00000425913.5:c.264_265delinsTG	ENSP00000393359.1:p.Phe88=
ENST00000429356.5:c.72_73delinsTG	ENSP00000398585.1:p.Phe24=
ENST00000445705.1:c.264_265delinsTG	ENSP00000398257.1:p.Phe88=
ENST00000459934.5:n.382_383delinsTG
ENST00000467493.5:n.724_725delinsTG
ENST00000470949.5:n.209_210delinsTG
ENST00000481736.5:n.668_669delinsTG
ENST00000486382.1:n.365_366delinsTG
ENST00000617979.4:c.264_265delinsTG	ENSP00000483375.1:p.Phe88=
NM_000403.3:c.264_265delinsTG	NP_000394.2:p.Phe88=
NM_001008216.1:c.264_265delinsTG	NP_001008217.1:p.Phe88=
NM_001127621.1:c.264_265delinsTG	NP_001121093.1:p.Phe88=
NM_001008216.2:c.264_265delinsTG MANE Select	NP_001008217.1:p.Phe88=
NM_000403.4:c.264_265delinsTG	NP_000394.2:p.Phe88=
NM_001127621.2:c.264_265delinsTG	NP_001121093.1:p.Phe88=