Canonical Allele Identifier: CA19282301

Gene: GALE

Linked Data

• dbSNP Id: rs1047792010
• MyVariant Identifiers: chr1:g.24124876_24124885del (hg19) ; chr1:g.23798386_23798395del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798388_23798397del , CM000663.2:g.23798388_23798397del	GRCh38
NC_000001.10:g.24124878_24124887del , CM000663.1:g.24124878_24124887del	GRCh37
NC_000001.9:g.23997465_23997474del	NCBI36
NG_007068.1:g.7410_7419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.238-165_238-156del MANE Select	ENSP00000483375.1:n.238-165_238-156del
ENST00000374497.7:c.238-165_238-156del	ENSP00000363621.3:n.238-165_238-156del
ENST00000418277.5:c.46-165_46-156del	ENSP00000414719.1:n.46-165_46-156del
ENST00000425913.5:c.238-165_238-156del	ENSP00000393359.1:n.238-165_238-156del
ENST00000429356.5:c.46-165_46-156del	ENSP00000398585.1:n.46-165_46-156del
ENST00000445705.1:c.238-165_238-156del	ENSP00000398257.1:n.238-165_238-156del
ENST00000459934.5:n.356-165_356-156del
ENST00000466250.5:n.583_592del
ENST00000467493.5:n.533_542del
ENST00000470383.1:n.2005_2014del
ENST00000470949.5:n.188-170_188-161del
ENST00000481736.5:n.477_486del
ENST00000486382.1:n.344-170_344-161del
ENST00000617979.4:c.238-165_238-156del	ENSP00000483375.1:n.238-165_238-156del
NM_000403.3:c.238-165_238-156del	NP_000394.2:n.238-165_238-156del
NM_001008216.1:c.238-165_238-156del	NP_001008217.1:n.238-165_238-156del
NM_001127621.1:c.238-165_238-156del	NP_001121093.1:n.238-165_238-156del
NM_001008216.2:c.238-165_238-156del MANE Select	NP_001008217.1:n.238-165_238-156del
NM_000403.4:c.238-165_238-156del	NP_000394.2:n.238-165_238-156del
NM_001127621.2:c.238-165_238-156del	NP_001121093.1:n.238-165_238-156del