Canonical Allele Identifier: CA2655002328

Gene: MCM3AP

Linked Data

• gnomAD v4: 21-46265891-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46265891C>T , CM000683.2:g.46265891C>T	GRCh38
NC_000021.8:g.47685805C>T , CM000683.1:g.47685805C>T	GRCh37
NC_000021.7:g.46510233C>T	NCBI36
NG_033881.1:g.24432G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291688.6:c.3031+34G>A MANE Select	ENSP00000291688.1:n.3031+34G>A
ENST00000291688.5:c.3031+34G>A	ENSP00000291688.1:n.3031+34G>A
ENST00000397708.1:c.3031+34G>A	ENSP00000380820.1:n.3031+34G>A
ENST00000486937.5:n.1323+34G>A
ENST00000496607.5:n.1028+34G>A
NM_003906.4:c.3031+34G>A	NP_003897.2:n.3031+34G>A
XM_005261203.3:c.3031+34G>A	XP_005261260.1:n.3031+34G>A
XM_005261204.3:c.3031+34G>A	XP_005261261.1:n.3031+34G>A
XM_005261205.2:c.3031+34G>A	XP_005261262.1:n.3031+34G>A
XM_005261206.3:c.3031+34G>A	XP_005261263.1:n.3031+34G>A
XM_006724064.2:c.3031+34G>A	XP_006724127.1:n.3031+34G>A
XR_937577.1:n.3620+34G>A
XM_005261203.4:c.3031+34G>A	XP_005261260.1:n.3031+34G>A
XM_005261204.5:c.3031+34G>A	XP_005261261.1:n.3031+34G>A
XM_005261205.4:c.3031+34G>A	XP_005261262.1:n.3031+34G>A
NM_003906.5:c.3031+34G>A MANE Select	NP_003897.2:n.3031+34G>A