Canonical Allele Identifier: CA10076033
Community Standard Title: NM_003906.5(MCM3AP):c.4704C>T (p.Cys1568=)
Gene: MCM3AP HGNC NCBI
MCM3AP-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46245141G>A , CM000683.2:g.46245141G>A GRCh38
NC_000021.8:g.47665055G>A , CM000683.1:g.47665055G>A GRCh37
NC_000021.7:g.46489483G>A NCBI36
NG_033881.1:g.45182C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003906.5:c.4704C>T (MCM3AP) MANE Select NP_003897.2:p.Cys1568=
ENST00000291688.6:c.4704C>T (MCM3AP) MANE Select ENSP00000291688.1:p.Cys1568=
NM_003906.4:c.4704C>T (MCM3AP) NP_003897.2:p.Cys1568=
NR_002776.4:n.222+4122G>A (MCM3AP-AS1)
NR_110565.1:n.423+4122G>A (MCM3AP-AS1)
ENST00000291688.5:c.4704C>T (MCM3AP) ENSP00000291688.1:p.Cys1568=
ENST00000397708.1:c.4704C>T (MCM3AP) ENSP00000380820.1:p.Cys1568=
ENST00000467026.5:n.1297C>T (MCM3AP)
ENST00000486937.5:n.3219C>T (MCM3AP)
ENST00000496607.5:n.2701C>T (MCM3AP)
XM_005261203.3:c.4704C>T (MCM3AP) XP_005261260.1:p.Cys1568=
XM_005261203.4:c.4704C>T (MCM3AP) XP_005261260.1:p.Cys1568=
XM_005261204.3:c.4704C>T (MCM3AP) XP_005261261.1:p.Cys1568=
XM_005261204.5:c.4704C>T (MCM3AP) XP_005261261.1:p.Cys1568=
XM_005261205.2:c.4704C>T (MCM3AP) XP_005261262.1:p.Cys1568=
XM_005261205.4:c.4704C>T (MCM3AP) XP_005261262.1:p.Cys1568=
XM_005261206.3:c.4704C>T (MCM3AP) XP_005261263.1:p.Cys1568=
XM_006724064.2:c.4704C>T (MCM3AP) XP_006724127.1:p.Cys1568=
XR_937577.1:n.5139C>T (MCM3AP)