Canonical Allele Identifier: CA2392584534

Gene: MCM3AP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46266123A= , CM000683.2:g.46266123A=	GRCh38
NC_000021.8:g.47686037A= , CM000683.1:g.47686037A=	GRCh37
NC_000021.7:g.46510465A=	NCBI36
NG_033881.1:g.24200T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291688.6:c.2833T= MANE Select	ENSP00000291688.1:p.Leu945=
ENST00000291688.5:c.2833T=	ENSP00000291688.1:p.Leu945=
ENST00000397708.1:c.2833T=	ENSP00000380820.1:p.Leu945=
ENST00000486937.5:n.1125T=
ENST00000496607.5:n.830T=
NM_003906.4:c.2833T=	NP_003897.2:p.Leu945=
XM_005261203.3:c.2833T=	XP_005261260.1:p.Leu945=
XM_005261204.3:c.2833T=	XP_005261261.1:p.Leu945=
XM_005261205.2:c.2833T=	XP_005261262.1:p.Leu945=
XM_005261206.3:c.2833T=	XP_005261263.1:p.Leu945=
XM_006724064.2:c.2833T=	XP_006724127.1:p.Leu945=
XR_937577.1:n.3422T=
XM_005261203.4:c.2833T=	XP_005261260.1:p.Leu945=
XM_005261204.5:c.2833T=	XP_005261261.1:p.Leu945=
XM_005261205.4:c.2833T=	XP_005261262.1:p.Leu945=
NM_003906.5:c.2833T= MANE Select	NP_003897.2:p.Leu945=