Canonical Allele Identifier: CA1158961470
Gene: GALE HGNC NCBI

Linked Data

dbSNP Id: rs1639025855

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23798290_23798293dup , CM000663.2:g.23798290_23798293dup GRCh38
NC_000001.10:g.24124780_24124783dup , CM000663.1:g.24124780_24124783dup GRCh37
NC_000001.9:g.23997367_23997370dup NCBI36
NG_007068.1:g.7513_7516dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.238-62_238-59dup MANE Select ENSP00000483375.1:n.238-62_238-59dup
ENST00000374497.7:c.238-62_238-59dup ENSP00000363621.3:n.238-62_238-59dup
ENST00000418277.5:c.46-62_46-59dup ENSP00000414719.1:n.46-62_46-59dup
ENST00000425913.5:c.238-62_238-59dup ENSP00000393359.1:n.238-62_238-59dup
ENST00000429356.5:c.46-62_46-59dup ENSP00000398585.1:n.46-62_46-59dup
ENST00000445705.1:c.238-62_238-59dup ENSP00000398257.1:n.238-62_238-59dup
ENST00000459934.5:n.356-62_356-59dup
ENST00000467493.5:n.636_639dup
ENST00000470949.5:n.188-67_188-64dup
ENST00000481736.5:n.580_583dup
ENST00000486382.1:n.344-67_344-64dup
ENST00000617979.4:c.238-62_238-59dup ENSP00000483375.1:n.238-62_238-59dup
NM_000403.3:c.238-62_238-59dup NP_000394.2:n.238-62_238-59dup
NM_001008216.1:c.238-62_238-59dup NP_001008217.1:n.238-62_238-59dup
NM_001127621.1:c.238-62_238-59dup NP_001121093.1:n.238-62_238-59dup
NM_001008216.2:c.238-62_238-59dup MANE Select NP_001008217.1:n.238-62_238-59dup
NM_000403.4:c.238-62_238-59dup NP_000394.2:n.238-62_238-59dup
NM_001127621.2:c.238-62_238-59dup NP_001121093.1:n.238-62_238-59dup