Canonical Allele Identifier: CA540074898

Gene: MROH2A

Linked Data

• dbSNP Id: rs1194312357
• gnomAD v2: 2-234687329-ACC-A
• gnomAD v3: 2-233778683-ACC-A
• gnomAD v4: 2-233778683-ACC-A
• MyVariant Identifiers: chr2:g.234687330_234687331del (hg19) ; chr2:g.233778684_233778685del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233778686_233778687del , CM000664.2:g.233778686_233778687del	GRCh38
NC_000002.11:g.234687332_234687333del , CM000664.1:g.234687332_234687333del	GRCh37
NC_000002.10:g.234352071_234352072del	NCBI36
NG_051337.1:g.8025_8026del

Transcript Alleles

HGVS	Amino-acid change
ENST00000389758.4:c.-15+205_-15+206del MANE Select	ENSP00000374408.3:n.-15+205_-15+206del
ENST00000389758.3:c.-15+205_-15+206del	ENSP00000374408.3:n.-15+205_-15+206del
ENST00000428446.5:c.-12-661_-12-660del	ENSP00000404614.1:n.-12-661_-12-660del
ENST00000430892.5:c.-14-659_-14-658del	ENSP00000392128.1:n.-14-659_-14-658del
ENST00000454283.1:c.-83-985_-83-984del	ENSP00000409355.1:n.-83-985_-83-984del
ENST00000610772.4:c.-14-659_-14-658del	ENSP00000477597.1:n.-14-659_-14-658del
NM_001287395.1:c.-14-659_-14-658del	NP_001274324.1:n.-14-659_-14-658del
XM_011511075.1:c.76+205_76+206del	XP_011509377.1:n.76+205_76+206del
XM_011511076.1:c.76+205_76+206del	XP_011509378.1:n.76+205_76+206del
XM_011511077.1:c.76+205_76+206del	XP_011509379.1:n.76+205_76+206del
XM_011511078.1:c.76+205_76+206del	XP_011509380.1:n.76+205_76+206del
XM_011511079.1:c.76+205_76+206del	XP_011509381.1:n.76+205_76+206del
XM_011511080.1:c.-14-659_-14-658del	XP_011509382.1:n.-14-659_-14-658del
XM_011511081.1:c.76+205_76+206del	XP_011509383.1:n.76+205_76+206del
XM_011511082.1:c.76+205_76+206del	XP_011509384.1:n.76+205_76+206del
XM_011511083.1:c.76+205_76+206del	XP_011509385.1:n.76+205_76+206del
XM_011511084.1:c.76+205_76+206del	XP_011509386.1:n.76+205_76+206del
XM_011511086.1:c.76+205_76+206del	XP_011509388.1:n.76+205_76+206del
XM_011511076.2:c.76+205_76+206del	XP_011509378.1:n.76+205_76+206del
XM_011511086.2:c.76+205_76+206del	XP_011509388.1:n.76+205_76+206del
XM_024452839.1:c.76+205_76+206del	XP_024308607.1:n.76+205_76+206del
XM_024452840.1:c.76+205_76+206del	XP_024308608.1:n.76+205_76+206del
XM_024452841.1:c.76+205_76+206del	XP_024308609.1:n.76+205_76+206del
XM_024452842.1:c.-14-659_-14-658del	XP_024308610.1:n.-14-659_-14-658del
XM_024452843.1:c.76+205_76+206del	XP_024308611.1:n.76+205_76+206del
XM_024452844.1:c.76+205_76+206del	XP_024308612.1:n.76+205_76+206del
XM_024452845.1:c.76+205_76+206del	XP_024308613.1:n.76+205_76+206del
XM_024452846.1:c.76+205_76+206del	XP_024308614.1:n.76+205_76+206del
NM_001367507.1:c.-14-659_-14-658del	NP_001354436.1:n.-14-659_-14-658del
NM_001394639.1:c.-15+205_-15+206del MANE Select	NP_001381568.1:n.-15+205_-15+206del