Canonical Allele Identifier: CA15995998

Gene: HORMAD2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30090837A>G , CM000684.2:g.30090837A>G	GRCh38
NC_000022.10:g.30486826A>G , CM000684.1:g.30486826A>G	GRCh37
NC_000022.9:g.28816826A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336726.11:c.-37-3079A>G MANE Select	ENSP00000336984.6:n.-37-3079A>G
ENST00000336726.10:c.-37-3079A>G	ENSP00000336984.6:n.-37-3079A>G
ENST00000403975.1:c.-37-3079A>G	ENSP00000385055.1:n.-37-3079A>G
ENST00000450612.5:c.-37-3079A>G	ENSP00000393415.1:n.-37-3079A>G
NM_152510.2:c.-37-3079A>G	NP_689723.1:n.-37-3079A>G
XM_006724147.2:c.-37-3079A>G	XP_006724210.2:n.-37-3079A>G
XM_011529913.1:c.-37-3079A>G	XP_011528215.1:n.-37-3079A>G
XM_011529914.1:c.-37-3079A>G	XP_011528216.1:n.-37-3079A>G
XM_011529915.1:c.-37-3079A>G	XP_011528217.1:n.-37-3079A>G
XM_011529916.1:c.-37-3079A>G	XP_011528218.1:n.-37-3079A>G
XM_011529917.1:c.-37-3079A>G	XP_011528219.1:n.-37-3079A>G
XM_011529918.1:c.-37-3079A>G	XP_011528220.1:n.-37-3079A>G
XM_011529919.1:c.-264-3079A>G	XP_011528221.1:n.-264-3079A>G
NM_001329457.1:c.-37-3079A>G	NP_001316386.1:n.-37-3079A>G
NM_001329458.1:c.-264-3079A>G	NP_001316387.1:n.-264-3079A>G
NM_152510.3:c.-37-3079A>G	NP_689723.1:n.-37-3079A>G
XM_011529914.2:c.-37-3079A>G	XP_011528216.1:n.-37-3079A>G
XM_011529917.3:c.-37-3079A>G	XP_011528219.1:n.-37-3079A>G
XM_017028621.1:c.-37-3079A>G	XP_016884110.1:n.-37-3079A>G
XM_017028622.1:c.-37-3079A>G	XP_016884111.1:n.-37-3079A>G
XM_017028624.1:c.-264-3079A>G	XP_016884113.1:n.-264-3079A>G
NM_001329457.2:c.-37-3079A>G	NP_001316386.1:n.-37-3079A>G
NM_001329458.2:c.-264-3079A>G	NP_001316387.1:n.-264-3079A>G
NM_152510.4:c.-37-3079A>G MANE Select	NP_689723.1:n.-37-3079A>G