Canonical Allele Identifier: CA2580609700

Gene: HORMAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30098382G>C , CM000684.2:g.30098382G>C	GRCh38
NC_000022.10:g.30494371G>C , CM000684.1:g.30494371G>C	GRCh37
NC_000022.9:g.28824371G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336726.11:c.52-470G>C MANE Select	ENSP00000336984.6:n.52-470G>C
ENST00000336726.10:c.52-470G>C	ENSP00000336984.6:n.52-470G>C
ENST00000403975.1:c.52-470G>C	ENSP00000385055.1:n.52-470G>C
ENST00000450612.5:c.52-470G>C	ENSP00000393415.1:n.52-470G>C
ENST00000491605.1:n.47-470G>C
NM_152510.2:c.52-470G>C	NP_689723.1:n.52-470G>C
XM_006724147.2:c.52-470G>C	XP_006724210.2:n.52-470G>C
XM_011529913.1:c.52-470G>C	XP_011528215.1:n.52-470G>C
XM_011529914.1:c.52-470G>C	XP_011528216.1:n.52-470G>C
XM_011529915.1:c.52-470G>C	XP_011528217.1:n.52-470G>C
XM_011529916.1:c.52-470G>C	XP_011528218.1:n.52-470G>C
XM_011529917.1:c.52-470G>C	XP_011528219.1:n.52-470G>C
XM_011529918.1:c.52-470G>C	XP_011528220.1:n.52-470G>C
XM_011529919.1:c.-176-470G>C	XP_011528221.1:n.-176-470G>C
NM_001329457.1:c.52-470G>C	NP_001316386.1:n.52-470G>C
NM_001329458.1:c.-176-470G>C	NP_001316387.1:n.-176-470G>C
NM_152510.3:c.52-470G>C	NP_689723.1:n.52-470G>C
XM_011529914.2:c.52-470G>C	XP_011528216.1:n.52-470G>C
XM_011529917.3:c.52-470G>C	XP_011528219.1:n.52-470G>C
XM_017028621.1:c.52-470G>C	XP_016884110.1:n.52-470G>C
XM_017028622.1:c.52-470G>C	XP_016884111.1:n.52-470G>C
XM_017028624.1:c.-176-470G>C	XP_016884113.1:n.-176-470G>C
NM_001329457.2:c.52-470G>C	NP_001316386.1:n.52-470G>C
NM_001329458.2:c.-176-470G>C	NP_001316387.1:n.-176-470G>C
NM_152510.4:c.52-470G>C MANE Select	NP_689723.1:n.52-470G>C