Canonical Allele Identifier: CA367213773

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36422716A>C , CM000669.2:g.36422716A>C	GRCh38
NC_000007.13:g.36462325A>C , CM000669.1:g.36462325A>C	GRCh37
NC_000007.12:g.36428850A>C	NCBI36
NG_041770.1:g.37914A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018685.5:c.2383A>C MANE Select	NP_061155.2:p.Ser795Arg
ENST00000265748.7:c.2383A>C MANE Select	ENSP00000265748.2:p.Ser795Arg
NM_001284301.2:c.2272A>C	NP_001271230.1:p.Ser758Arg
NM_001284301.3:c.2272A>C	NP_001271230.1:p.Ser758Arg
NM_001284302.2:c.2269A>C	NP_001271231.1:p.Ser757Arg
NM_001284302.3:c.2269A>C	NP_001271231.1:p.Ser757Arg
NM_018685.4:c.2383A>C	NP_061155.2:p.Ser795Arg
ENST00000265748.6:c.2383A>C	ENSP00000265748.2:p.Ser795Arg
ENST00000396068.6:c.2272A>C	ENSP00000379380.2:p.Ser758Arg
ENST00000428612.5:c.97-1829A>C
ENST00000446635.5:c.444A>C
XM_006715746.1:c.2383A>C	XP_006715809.1:p.Ser795Arg
XM_006715746.2:c.2383A>C	XP_006715809.1:p.Ser795Arg
XM_006715747.2:c.2272A>C	XP_006715810.1:p.Ser758Arg
XM_006715747.4:c.2272A>C	XP_006715810.1:p.Ser758Arg
XM_017012354.2:c.2371A>C	XP_016867843.1:p.Ser791Arg
XM_017012355.2:c.2371A>C	XP_016867844.1:p.Ser791Arg
XM_017012356.2:c.2260A>C	XP_016867845.1:p.Ser754Arg