Canonical Allele Identifier: CA4220126

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36449868A>G , CM000669.2:g.36449868A>G	GRCh38
NC_000007.13:g.36489477A>G , CM000669.1:g.36489477A>G	GRCh37
NC_000007.12:g.36456002A>G	NCBI36
NG_041770.1:g.65066A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265748.7:c.3251+31A>G MANE Select	ENSP00000265748.2:n.3251+31A>G
ENST00000265748.6:c.3251+31A>G	ENSP00000265748.2:n.3251+31A>G
ENST00000396068.6:c.3140+31A>G	ENSP00000379380.2:n.3140+31A>G
ENST00000491782.1:n.899+31A>G
NM_001284301.2:c.3140+31A>G	NP_001271230.1:n.3140+31A>G
NM_001284302.2:c.3137+31A>G	NP_001271231.1:n.3137+31A>G
NM_018685.4:c.3251+31A>G	NP_061155.2:n.3251+31A>G
XM_006715746.1:c.3305+31A>G	XP_006715809.1:n.3305+31A>G
XM_006715747.2:c.3194+31A>G	XP_006715810.1:n.3194+31A>G
XM_006715746.2:c.3305+31A>G	XP_006715809.1:n.3305+31A>G
XM_006715747.4:c.3194+31A>G	XP_006715810.1:n.3194+31A>G
XM_017012354.2:c.3293+31A>G	XP_016867843.1:n.3293+31A>G
XM_017012355.2:c.3239+31A>G	XP_016867844.1:n.3239+31A>G
XM_017012356.2:c.3128+31A>G	XP_016867845.1:n.3128+31A>G
NM_018685.5:c.3251+31A>G MANE Select	NP_061155.2:n.3251+31A>G
NM_001284301.3:c.3140+31A>G	NP_001271230.1:n.3140+31A>G
NM_001284302.3:c.3137+31A>G	NP_001271231.1:n.3137+31A>G