Canonical Allele Identifier: CA4219373

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36406246A>C , CM000669.2:g.36406246A>C	GRCh38
NC_000007.13:g.36445855A>C , CM000669.1:g.36445855A>C	GRCh37
NC_000007.12:g.36412380A>C	NCBI36
NG_041770.1:g.21444A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018685.5:c.553A>C MANE Select	NP_061155.2:p.Arg185=
ENST00000265748.7:c.553A>C MANE Select	ENSP00000265748.2:p.Arg185=
NM_001284301.2:c.553A>C	NP_001271230.1:p.Arg185=
NM_001284301.3:c.553A>C	NP_001271230.1:p.Arg185=
NM_001284302.2:c.553A>C	NP_001271231.1:p.Arg185=
NM_001284302.3:c.553A>C	NP_001271231.1:p.Arg185=
NM_018685.4:c.553A>C	NP_061155.2:p.Arg185=
ENST00000265748.6:c.553A>C	ENSP00000265748.2:p.Arg185=
ENST00000396068.6:c.553A>C	ENSP00000379380.2:p.Arg185=
ENST00000424865.1:c.487A>C	ENSP00000404979.1:p.Arg163=
ENST00000460598.1:n.140A>C
XM_006715746.1:c.553A>C	XP_006715809.1:p.Arg185=
XM_006715746.2:c.553A>C	XP_006715809.1:p.Arg185=
XM_006715747.2:c.553A>C	XP_006715810.1:p.Arg185=
XM_006715747.4:c.553A>C	XP_006715810.1:p.Arg185=
XM_017012354.2:c.553A>C	XP_016867843.1:p.Arg185=
XM_017012355.2:c.553A>C	XP_016867844.1:p.Arg185=
XM_017012356.2:c.553A>C	XP_016867845.1:p.Arg185=