Canonical Allele Identifier: CA2400890138

Gene: HORMAD2

Linked Data

• dbSNP Id: rs1923432425

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30133577G>T , CM000684.2:g.30133577G>T	GRCh38
NC_000022.10:g.30529566G>T , CM000684.1:g.30529566G>T	GRCh37
NC_000022.9:g.28859566G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336726.11:c.819+11363G>T MANE Select	ENSP00000336984.6:n.819+11363G>T
ENST00000336726.10:c.819+11363G>T	ENSP00000336984.6:n.819+11363G>T
ENST00000403975.1:c.819+11363G>T	ENSP00000385055.1:n.819+11363G>T
NM_152510.2:c.819+11363G>T	NP_689723.1:n.819+11363G>T
XM_006724147.2:c.819+11363G>T	XP_006724210.2:n.819+11363G>T
XM_011529913.1:c.819+11363G>T	XP_011528215.1:n.819+11363G>T
XM_011529914.1:c.819+11363G>T	XP_011528216.1:n.819+11363G>T
XM_011529915.1:c.819+11363G>T	XP_011528217.1:n.819+11363G>T
XM_011529916.1:c.819+11363G>T	XP_011528218.1:n.819+11363G>T
XM_011529917.1:c.819+11363G>T	XP_011528219.1:n.819+11363G>T
XM_011529919.1:c.555+11363G>T	XP_011528221.1:n.555+11363G>T
NM_001329457.1:c.819+11363G>T	NP_001316386.1:n.819+11363G>T
NM_001329458.1:c.555+11363G>T	NP_001316387.1:n.555+11363G>T
NM_152510.3:c.819+11363G>T	NP_689723.1:n.819+11363G>T
XM_011529914.2:c.819+11363G>T	XP_011528216.1:n.819+11363G>T
XM_011529917.3:c.819+11363G>T	XP_011528219.1:n.819+11363G>T
XM_017028621.1:c.819+11363G>T	XP_016884110.1:n.819+11363G>T
XM_017028622.1:c.819+11363G>T	XP_016884111.1:n.819+11363G>T
XM_017028624.1:c.555+11363G>T	XP_016884113.1:n.555+11363G>T
XM_017028625.1:c.507+11363G>T	XP_016884114.1:n.507+11363G>T
XM_017028626.1:c.417+11363G>T	XP_016884115.1:n.417+11363G>T
NM_001329457.2:c.819+11363G>T	NP_001316386.1:n.819+11363G>T
NM_001329458.2:c.555+11363G>T	NP_001316387.1:n.555+11363G>T
NM_152510.4:c.819+11363G>T MANE Select	NP_689723.1:n.819+11363G>T