Canonical Allele Identifier: CA1080032

Gene: HORMAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150711564G>A , CM000663.2:g.150711564G>A	GRCh38
NC_000001.10:g.150684040G>A , CM000663.1:g.150684040G>A	GRCh37
NC_000001.9:g.148950664G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032132.5:c.308C>T MANE Select	NP_115508.2:p.Thr103Ile
ENST00000361824.7:c.308C>T MANE Select	ENSP00000355167.2:p.Thr103Ile
NM_001199829.1:c.287C>T	NP_001186758.1:p.Thr96Ile
NM_001199829.2:c.287C>T	NP_001186758.1:p.Thr96Ile
NM_032132.4:c.308C>T	NP_115508.2:p.Thr103Ile
ENST00000322343.11:c.287C>T	ENSP00000326489.7:p.Thr96Ile
ENST00000361824.6:c.308C>T	ENSP00000355167.2:p.Thr103Ile
ENST00000368987.5:c.95C>T	ENSP00000357983.1:p.Thr32Ile
ENST00000368995.8:c.87+269C>T	ENSP00000357991.4:n.87+269C>T
ENST00000442853.5:c.74C>T	ENSP00000401940.1:p.Thr25Ile
XM_006711569.2:c.308C>T	XP_006711632.1:p.Thr103Ile
XM_006711570.2:c.95C>T	XP_006711633.1:p.Thr32Ile
XM_006711571.2:c.74C>T	XP_006711634.1:p.Thr25Ile
XM_011510053.1:c.308C>T	XP_011508355.1:p.Thr103Ile
XM_011510054.1:c.308C>T	XP_011508356.1:p.Thr103Ile
XM_011510054.2:c.308C>T	XP_011508356.1:p.Thr103Ile
XM_011510055.1:c.65C>T	XP_011508357.1:p.Thr22Ile
XM_011510056.1:c.11C>T	XP_011508358.1:p.Thr4Ile