Canonical Allele Identifier: CA1979318303

Gene: SIPA1

Linked Data

• dbSNP Id: rs2448490

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65644564G>C , CM000673.2:g.65644564G>C	GRCh38
NC_000011.9:g.65412035G>C , CM000673.1:g.65412035G>C	GRCh37
NC_000011.8:g.65168611G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000534313.6:c.985-391G>C MANE Select	ENSP00000436269.1:n.985-391G>C
ENST00000394224.3:c.985-391G>C	ENSP00000377771.3:n.985-391G>C
ENST00000394227.7:c.985-391G>C	ENSP00000377774.4:n.985-391G>C
ENST00000527525.5:c.985-391G>C	ENSP00000433686.1:n.985-391G>C
ENST00000534313.5:c.985-391G>C	ENSP00000436269.1:n.985-391G>C
ENST00000628801.2:c.985-391G>C	ENSP00000485899.1:n.985-391G>C
NM_006747.3:c.985-391G>C	NP_006738.3:n.985-391G>C
NM_153253.29:c.985-391G>C	NP_694985.29:n.985-391G>C
XM_005274189.2:c.985-391G>C	XP_005274246.1:n.985-391G>C
XM_011545214.1:c.985-391G>C	XP_011543516.1:n.985-391G>C
XR_247210.2:n.1094-391G>C
XR_950017.1:n.1094-391G>C
NM_006747.4:c.985-391G>C MANE Select	NP_006738.3:n.985-391G>C
NM_153253.30:c.985-391G>C	NP_694985.29:n.985-391G>C