Canonical Allele Identifier: CA2400872494

Gene: HORMAD2

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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