Canonical Allele Identifier: CA2392584415

Gene: MCM3AP

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46265873_46265874delinsTC , CM000683.2:g.46265873_46265874delinsTC	GRCh38
NC_000021.8:g.47685787_47685788delinsTC , CM000683.1:g.47685787_47685788delinsTC	GRCh37
NC_000021.7:g.46510215_46510216delinsTC	NCBI36
NG_033881.1:g.24449_24450delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291688.6:c.3031+51_3031+52delinsGA MANE Select	ENSP00000291688.1:n.3031+51_3031+52delinsGA
ENST00000291688.5:c.3031+51_3031+52delinsGA	ENSP00000291688.1:n.3031+51_3031+52delinsGA
ENST00000397708.1:c.3031+51_3031+52delinsGA	ENSP00000380820.1:n.3031+51_3031+52delinsGA
ENST00000486937.5:n.1323+51_1323+52delinsGA
ENST00000496607.5:n.1028+51_1028+52delinsGA
NM_003906.4:c.3031+51_3031+52delinsGA	NP_003897.2:n.3031+51_3031+52delinsGA
XM_005261203.3:c.3031+51_3031+52delinsGA	XP_005261260.1:n.3031+51_3031+52delinsGA
XM_005261204.3:c.3031+51_3031+52delinsGA	XP_005261261.1:n.3031+51_3031+52delinsGA
XM_005261205.2:c.3031+51_3031+52delinsGA	XP_005261262.1:n.3031+51_3031+52delinsGA
XM_005261206.3:c.3031+51_3031+52delinsGA	XP_005261263.1:n.3031+51_3031+52delinsGA
XM_006724064.2:c.3031+51_3031+52delinsGA	XP_006724127.1:n.3031+51_3031+52delinsGA
XR_937577.1:n.3620+51_3620+52delinsGA
XM_005261203.4:c.3031+51_3031+52delinsGA	XP_005261260.1:n.3031+51_3031+52delinsGA
XM_005261204.5:c.3031+51_3031+52delinsGA	XP_005261261.1:n.3031+51_3031+52delinsGA
XM_005261205.4:c.3031+51_3031+52delinsGA	XP_005261262.1:n.3031+51_3031+52delinsGA
NM_003906.5:c.3031+51_3031+52delinsGA MANE Select	NP_003897.2:n.3031+51_3031+52delinsGA