Canonical Allele Identifier: CA2655002355

Gene: MCM3AP

Linked Data

• gnomAD v4: 21-46266035-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46266036dup , CM000683.2:g.46266036dup	GRCh38
NC_000021.8:g.47685950dup , CM000683.1:g.47685950dup	GRCh37
NC_000021.7:g.46510378dup	NCBI36
NG_033881.1:g.24287dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291688.6:c.2920dup MANE Select	ENSP00000291688.1:p.Val974GlyfsTer?
ENST00000291688.5:c.2920dup	ENSP00000291688.1:p.Val974GlyfsTer?
ENST00000397708.1:c.2920dup	ENSP00000380820.1:p.Val974GlyfsTer?
ENST00000486937.5:n.1212dup
ENST00000496607.5:n.917dup
NM_003906.4:c.2920dup	NP_003897.2:p.Val974GlyfsTer?
XM_005261203.3:c.2920dup	XP_005261260.1:p.Val974GlyfsTer?
XM_005261204.3:c.2920dup	XP_005261261.1:p.Val974GlyfsTer?
XM_005261205.2:c.2920dup	XP_005261262.1:p.Val974GlyfsTer?
XM_005261206.3:c.2920dup	XP_005261263.1:p.Val974GlyfsTer?
XM_006724064.2:c.2920dup	XP_006724127.1:p.Val974GlyfsTer?
XR_937577.1:n.3509dup
XM_005261203.4:c.2920dup	XP_005261260.1:p.Val974GlyfsTer?
XM_005261204.5:c.2920dup	XP_005261261.1:p.Val974GlyfsTer?
XM_005261205.4:c.2920dup	XP_005261262.1:p.Val974GlyfsTer?
NM_003906.5:c.2920dup MANE Select	NP_003897.2:p.Val974GlyfsTer?