Canonical Allele Identifier: CA1979315484
Community Standard Title: NM_006747.4(SIPA1):c.316G= (p.Ala106=)
Gene: SIPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65641237G= , CM000673.2:g.65641237G= GRCh38
NC_000011.9:g.65408708G= , CM000673.1:g.65408708G= GRCh37
NC_000011.8:g.65165284G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006747.4:c.316G= MANE Select NP_006738.3:p.Ala106=
ENST00000534313.6:c.316G= MANE Select ENSP00000436269.1:p.Ala106=
NM_006747.3:c.316G= NP_006738.3:p.Ala106=
NM_153253.29:c.316G= NP_694985.29:p.Ala106=
NM_153253.30:c.316G= NP_694985.29:p.Ala106=
ENST00000394224.3:c.316G= ENSP00000377771.3:p.Ala106=
ENST00000394227.7:c.316G= ENSP00000377774.4:p.Ala106=
ENST00000527525.5:c.316G= ENSP00000433686.1:p.Ala106=
ENST00000534313.5:c.316G= ENSP00000436269.1:p.Ala106=
ENST00000628801.2:c.316G= ENSP00000485899.1:p.Ala106=
XM_005274189.2:c.316G= XP_005274246.1:p.Ala106=
XM_011545214.1:c.316G= XP_011543516.1:p.Ala106=
XR_247210.2:n.425G=
XR_950017.1:n.425G=