Canonical Allele Identifier: CA2392584443

Gene: MCM3AP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46265933T= , CM000683.2:g.46265933T=	GRCh38
NC_000021.8:g.47685847T= , CM000683.1:g.47685847T=	GRCh37
NC_000021.7:g.46510275T=	NCBI36
NG_033881.1:g.24390A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291688.6:c.3023A= MANE Select	ENSP00000291688.1:p.Asp1008=
ENST00000291688.5:c.3023A=	ENSP00000291688.1:p.Asp1008=
ENST00000397708.1:c.3023A=	ENSP00000380820.1:p.Asp1008=
ENST00000486937.5:n.1315A=
ENST00000496607.5:n.1020A=
NM_003906.4:c.3023A=	NP_003897.2:p.Asp1008=
XM_005261203.3:c.3023A=	XP_005261260.1:p.Asp1008=
XM_005261204.3:c.3023A=	XP_005261261.1:p.Asp1008=
XM_005261205.2:c.3023A=	XP_005261262.1:p.Asp1008=
XM_005261206.3:c.3023A=	XP_005261263.1:p.Asp1008=
XM_006724064.2:c.3023A=	XP_006724127.1:p.Asp1008=
XR_937577.1:n.3612A=
XM_005261203.4:c.3023A=	XP_005261260.1:p.Asp1008=
XM_005261204.5:c.3023A=	XP_005261261.1:p.Asp1008=
XM_005261205.4:c.3023A=	XP_005261262.1:p.Asp1008=
NM_003906.5:c.3023A= MANE Select	NP_003897.2:p.Asp1008=