Canonical Allele Identifier: CA1979318333
Gene: SIPA1 HGNC NCBI

Linked Data

dbSNP Id: rs1856071060

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65644612del , CM000673.2:g.65644612del GRCh38
NC_000011.9:g.65412083del , CM000673.1:g.65412083del GRCh37
NC_000011.8:g.65168659del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000534313.6:c.985-343del MANE Select ENSP00000436269.1:n.985-343del
ENST00000394224.3:c.985-343del ENSP00000377771.3:n.985-343del
ENST00000394227.7:c.985-343del ENSP00000377774.4:n.985-343del
ENST00000527525.5:c.985-343del ENSP00000433686.1:n.985-343del
ENST00000534313.5:c.985-343del ENSP00000436269.1:n.985-343del
ENST00000628801.2:c.985-343del ENSP00000485899.1:n.985-343del
NM_006747.3:c.985-343del NP_006738.3:n.985-343del
NM_153253.29:c.985-343del NP_694985.29:n.985-343del
XM_005274189.2:c.985-343del XP_005274246.1:n.985-343del
XM_011545214.1:c.985-343del XP_011543516.1:n.985-343del
XR_247210.2:n.1094-343del
XR_950017.1:n.1094-343del
NM_006747.4:c.985-343del MANE Select NP_006738.3:n.985-343del
NM_153253.30:c.985-343del NP_694985.29:n.985-343del