Canonical Allele Identifier: CA685516
Gene: GALE HGNC NCBI

Linked Data

dbSNP Id: rs764669674
gnomAD v2: 1-24123048-T-G
gnomAD v3: 1-23796558-T-G
gnomAD v4: 1-23796558-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23796558T>G , CM000663.2:g.23796558T>G GRCh38
NC_000001.10:g.24123048T>G , CM000663.1:g.24123048T>G GRCh37
NC_000001.9:g.23995635T>G NCBI36
NG_007068.1:g.9247A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000617979.5:c.824A>C MANE Select ENSP00000483375.1:p.Tyr275Ser
ENST00000374497.7:c.824A>C ENSP00000363621.3:p.Tyr275Ser
ENST00000418277.5:c.632A>C ENSP00000414719.1:p.Tyr211Ser
ENST00000429356.5:c.603+139A>C ENSP00000398585.1:n.603+139A>C
ENST00000456977.5:c.153+139A>C ENSP00000397045.1:n.153+139A>C
ENST00000459934.5:n.1052A>C
ENST00000469556.1:n.328A>C
ENST00000481736.5:n.1228A>C
ENST00000617979.4:c.824A>C ENSP00000483375.1:p.Tyr275Ser
NM_000403.3:c.824A>C NP_000394.2:p.Tyr275Ser
NM_001008216.1:c.824A>C NP_001008217.1:p.Tyr275Ser
NM_001127621.1:c.824A>C NP_001121093.1:p.Tyr275Ser
NM_001008216.2:c.824A>C MANE Select NP_001008217.1:p.Tyr275Ser
NM_000403.4:c.824A>C NP_000394.2:p.Tyr275Ser
NM_001127621.2:c.824A>C NP_001121093.1:p.Tyr275Ser