Canonical Allele Identifier: CA410561832

Gene: MCM3AP

Linked Data

• MyVariant Identifiers: chr21:g.47685997A>T (hg19) ; chr21:g.46266083A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46266083A>T , CM000683.2:g.46266083A>T	GRCh38
NC_000021.8:g.47685997A>T , CM000683.1:g.47685997A>T	GRCh37
NC_000021.7:g.46510425A>T	NCBI36
NG_033881.1:g.24240T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291688.6:c.2873T>A MANE Select	ENSP00000291688.1:p.Leu958Gln
ENST00000291688.5:c.2873T>A	ENSP00000291688.1:p.Leu958Gln
ENST00000397708.1:c.2873T>A	ENSP00000380820.1:p.Leu958Gln
ENST00000486937.5:n.1165T>A
ENST00000496607.5:n.870T>A
NM_003906.4:c.2873T>A	NP_003897.2:p.Leu958Gln
XM_005261203.3:c.2873T>A	XP_005261260.1:p.Leu958Gln
XM_005261204.3:c.2873T>A	XP_005261261.1:p.Leu958Gln
XM_005261205.2:c.2873T>A	XP_005261262.1:p.Leu958Gln
XM_005261206.3:c.2873T>A	XP_005261263.1:p.Leu958Gln
XM_006724064.2:c.2873T>A	XP_006724127.1:p.Leu958Gln
XR_937577.1:n.3462T>A
XM_005261203.4:c.2873T>A	XP_005261260.1:p.Leu958Gln
XM_005261204.5:c.2873T>A	XP_005261261.1:p.Leu958Gln
XM_005261205.4:c.2873T>A	XP_005261262.1:p.Leu958Gln
NM_003906.5:c.2873T>A MANE Select	NP_003897.2:p.Leu958Gln