Canonical Allele Identifier: CA1335899866

Gene: MROH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233778718_233778719delinsAT , CM000664.2:g.233778718_233778719delinsAT	GRCh38
NC_000002.11:g.234687364_234687365delinsAT , CM000664.1:g.234687364_234687365delinsAT	GRCh37
NC_000002.10:g.234352103_234352104delinsAT	NCBI36
NG_051337.1:g.8057_8058delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000389758.4:c.-15+237_-15+238delinsAT MANE Select	ENSP00000374408.3:n.-15+237_-15+238delins...
ENST00000389758.3:c.-15+237_-15+238delinsAT	ENSP00000374408.3:n.-15+237_-15+238delins...
ENST00000428446.5:c.-12-629_-12-628delinsAT	ENSP00000404614.1:n.-12-629_-12-628delins...
ENST00000430892.5:c.-14-627_-14-626delinsAT	ENSP00000392128.1:n.-14-627_-14-626delins...
ENST00000454283.1:c.-83-953_-83-952delinsAT	ENSP00000409355.1:n.-83-953_-83-952delins...
ENST00000610772.4:c.-14-627_-14-626delinsAT	ENSP00000477597.1:n.-14-627_-14-626delins...
NM_001287395.1:c.-14-627_-14-626delinsAT	NP_001274324.1:n.-14-627_-14-626delinsAT
XM_011511075.1:c.76+237_76+238delinsAT	XP_011509377.1:n.76+237_76+238delinsAT
XM_011511076.1:c.76+237_76+238delinsAT	XP_011509378.1:n.76+237_76+238delinsAT
XM_011511077.1:c.76+237_76+238delinsAT	XP_011509379.1:n.76+237_76+238delinsAT
XM_011511078.1:c.76+237_76+238delinsAT	XP_011509380.1:n.76+237_76+238delinsAT
XM_011511079.1:c.76+237_76+238delinsAT	XP_011509381.1:n.76+237_76+238delinsAT
XM_011511080.1:c.-14-627_-14-626delinsAT	XP_011509382.1:n.-14-627_-14-626delinsAT
XM_011511081.1:c.76+237_76+238delinsAT	XP_011509383.1:n.76+237_76+238delinsAT
XM_011511082.1:c.76+237_76+238delinsAT	XP_011509384.1:n.76+237_76+238delinsAT
XM_011511083.1:c.76+237_76+238delinsAT	XP_011509385.1:n.76+237_76+238delinsAT
XM_011511084.1:c.76+237_76+238delinsAT	XP_011509386.1:n.76+237_76+238delinsAT
XM_011511086.1:c.76+237_76+238delinsAT	XP_011509388.1:n.76+237_76+238delinsAT
XM_011511076.2:c.76+237_76+238delinsAT	XP_011509378.1:n.76+237_76+238delinsAT
XM_011511086.2:c.76+237_76+238delinsAT	XP_011509388.1:n.76+237_76+238delinsAT
XM_024452839.1:c.76+237_76+238delinsAT	XP_024308607.1:n.76+237_76+238delinsAT
XM_024452840.1:c.76+237_76+238delinsAT	XP_024308608.1:n.76+237_76+238delinsAT
XM_024452841.1:c.76+237_76+238delinsAT	XP_024308609.1:n.76+237_76+238delinsAT
XM_024452842.1:c.-14-627_-14-626delinsAT	XP_024308610.1:n.-14-627_-14-626delinsAT
XM_024452843.1:c.76+237_76+238delinsAT	XP_024308611.1:n.76+237_76+238delinsAT
XM_024452844.1:c.76+237_76+238delinsAT	XP_024308612.1:n.76+237_76+238delinsAT
XM_024452845.1:c.76+237_76+238delinsAT	XP_024308613.1:n.76+237_76+238delinsAT
XM_024452846.1:c.76+237_76+238delinsAT	XP_024308614.1:n.76+237_76+238delinsAT
NM_001367507.1:c.-14-627_-14-626delinsAT	NP_001354436.1:n.-14-627_-14-626delinsAT
NM_001394639.1:c.-15+237_-15+238delinsAT MANE Select	NP_001381568.1:n.-15+237_-15+238delinsAT