Canonical Allele Identifier: CA2577631997

Gene: MCM3AP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46265928_46265929del , CM000683.2:g.46265928_46265929del	GRCh38
NC_000021.8:g.47685842_47685843del , CM000683.1:g.47685842_47685843del	GRCh37
NC_000021.7:g.46510270_46510271del	NCBI36
NG_033881.1:g.24394_24395del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291688.6:c.3027_3028del MANE Select	ENSP00000291688.1:p.Val1010GlyfsTer?
ENST00000291688.5:c.3027_3028del	ENSP00000291688.1:p.Val1010GlyfsTer?
ENST00000397708.1:c.3027_3028del	ENSP00000380820.1:p.Val1010GlyfsTer?
ENST00000486937.5:n.1319_1320del
ENST00000496607.5:n.1024_1025del
NM_003906.4:c.3027_3028del	NP_003897.2:p.Val1010GlyfsTer?
XM_005261203.3:c.3027_3028del	XP_005261260.1:p.Val1010GlyfsTer?
XM_005261204.3:c.3027_3028del	XP_005261261.1:p.Val1010GlyfsTer?
XM_005261205.2:c.3027_3028del	XP_005261262.1:p.Val1010GlyfsTer?
XM_005261206.3:c.3027_3028del	XP_005261263.1:p.Val1010GlyfsTer?
XM_006724064.2:c.3027_3028del	XP_006724127.1:p.Val1010GlyfsTer?
XR_937577.1:n.3616_3617del
XM_005261203.4:c.3027_3028del	XP_005261260.1:p.Val1010GlyfsTer?
XM_005261204.5:c.3027_3028del	XP_005261261.1:p.Val1010GlyfsTer?
XM_005261205.4:c.3027_3028del	XP_005261262.1:p.Val1010GlyfsTer?
NM_003906.5:c.3027_3028del MANE Select	NP_003897.2:p.Val1010GlyfsTer?