Canonical Allele Identifier: CA1149140209
Gene: GALE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23796488_23796499delinsGGGTGGGGCGGG , CM000663.2:g.23796488_23796499delinsGGGTGGGGCGGG GRCh38
NC_000001.10:g.24122978_24122989delinsGGGTGGGGCGGG , CM000663.1:g.24122978_24122989delinsGGGTGGGGCGGG GRCh37
NC_000001.9:g.23995565_23995576delinsGGGTGGGGCGGG NCBI36
NG_007068.1:g.9306_9317delinsCCCGCCCCACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.873+10_873+21delinsCCCGCCCCACCC MANE Select ENSP00000483375.1:n.873+10_873+21delinsCCCGCCCCACCC
ENST00000374497.7:c.873+10_873+21delinsCCCGCCCCACCC ENSP00000363621.3:n.873+10_873+21delinsCCCGCCCCACCC
ENST00000429356.5:c.603+198_603+209delinsCCCGCCCCACCC ENSP00000398585.1:n.603+198_603+209delinsCCCGCCCCACCC
ENST00000456977.5:c.153+198_153+209delinsCCCGCCCCACCC ENSP00000397045.1:n.153+198_153+209delinsCCCGCCCCACCC
ENST00000459934.5:n.1101+10_1101+21delinsCCCGCCCCACCC
ENST00000469556.1:n.387_398delinsCCCGCCCCACCC
ENST00000481736.5:n.1277+10_1277+21delinsCCCGCCCCACCC
ENST00000617979.4:c.873+10_873+21delinsCCCGCCCCACCC ENSP00000483375.1:n.873+10_873+21delinsCCCGCCCCACCC
NM_000403.3:c.873+10_873+21delinsCCCGCCCCACCC NP_000394.2:n.873+10_873+21delinsCCCGCCCCACCC
NM_001008216.1:c.873+10_873+21delinsCCCGCCCCACCC NP_001008217.1:n.873+10_873+21delinsCCCGCCCCACCC
NM_001127621.1:c.873+10_873+21delinsCCCGCCCCACCC NP_001121093.1:n.873+10_873+21delinsCCCGCCCCACCC
NM_001008216.2:c.873+10_873+21delinsCCCGCCCCACCC MANE Select NP_001008217.1:n.873+10_873+21delinsCCCGCCCCACCC
NM_000403.4:c.873+10_873+21delinsCCCGCCCCACCC NP_000394.2:n.873+10_873+21delinsCCCGCCCCACCC
NM_001127621.2:c.873+10_873+21delinsCCCGCCCCACCC NP_001121093.1:n.873+10_873+21delinsCCCGCCCCACCC