Canonical Allele Identifier: CA2171465869

Gene: FSIP1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39746232T>G , CM000677.2:g.39746232T>G	GRCh38
NC_000015.9:g.40038433T>G , CM000677.1:g.40038433T>G	GRCh37
NC_000015.8:g.37825725T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350221.4:c.560-4332A>C MANE Select	ENSP00000280236.3:n.560-4332A>C
ENST00000350221.3:c.560-4332A>C	ENSP00000280236.3:n.560-4332A>C
ENST00000559692.1:n.146+1070A>C
NM_152597.4:c.560-4332A>C	NP_689810.3:n.560-4332A>C
XM_005254208.2:c.560-4332A>C	XP_005254265.1:n.560-4332A>C
XM_011521305.1:c.560-4332A>C	XP_011519607.1:n.560-4332A>C
XM_011521306.1:c.560-4332A>C	XP_011519608.1:n.560-4332A>C
XM_011521307.1:c.560-4332A>C	XP_011519609.1:n.560-4332A>C
XM_011521308.1:c.560-4332A>C	XP_011519610.1:n.560-4332A>C
XM_011521309.1:c.560-4332A>C	XP_011519611.1:n.560-4332A>C
XM_011521310.1:c.560-4332A>C	XP_011519612.1:n.560-4332A>C
XM_011521311.1:c.-71-4332A>C	XP_011519613.1:n.-71-4332A>C
NM_001324338.1:c.560-4332A>C	NP_001311267.1:n.560-4332A>C
XM_011521305.3:c.560-4332A>C	XP_011519607.1:n.560-4332A>C
XM_011521306.2:c.560-4332A>C	XP_011519608.1:n.560-4332A>C
XM_011521307.3:c.560-4332A>C	XP_011519609.1:n.560-4332A>C
XM_011521309.3:c.560-4332A>C	XP_011519611.1:n.560-4332A>C
XM_011521311.3:c.-71-4332A>C	XP_011519613.1:n.-71-4332A>C
XM_017021972.2:c.-72+1070A>C	XP_016877461.1:n.-72+1070A>C
NM_152597.5:c.560-4332A>C MANE Select	NP_689810.3:n.560-4332A>C
NM_001324338.2:c.560-4332A>C	NP_001311267.1:n.560-4332A>C