Canonical Allele Identifier: CA513171969

Gene: MCM3AP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46284134G>A , CM000683.2:g.46284134G>A	GRCh38
NC_000021.8:g.47704048G>A , CM000683.1:g.47704048G>A	GRCh37
NC_000021.7:g.46528476G>A	NCBI36
NG_033881.1:g.6189C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003906.5:c.1153C>T MANE Select	NP_003897.2:p.Leu385=
ENST00000291688.6:c.1153C>T MANE Select	ENSP00000291688.1:p.Leu385=
NM_003906.4:c.1153C>T	NP_003897.2:p.Leu385=
ENST00000291688.5:c.1153C>T	ENSP00000291688.1:p.Leu385=
ENST00000397708.1:c.1153C>T	ENSP00000380820.1:p.Leu385=
XM_005261203.3:c.1153C>T	XP_005261260.1:p.Leu385=
XM_005261203.4:c.1153C>T	XP_005261260.1:p.Leu385=
XM_005261204.3:c.1153C>T	XP_005261261.1:p.Leu385=
XM_005261204.5:c.1153C>T	XP_005261261.1:p.Leu385=
XM_005261205.2:c.1153C>T	XP_005261262.1:p.Leu385=
XM_005261205.4:c.1153C>T	XP_005261262.1:p.Leu385=
XM_005261206.3:c.1153C>T	XP_005261263.1:p.Leu385=
XM_006724064.2:c.1153C>T	XP_006724127.1:p.Leu385=
XR_937577.1:n.1742C>T