Canonical Allele Identifier: CA2648555336

Gene: OR10Z1 SPTA1

Linked Data

• gnomAD v4: 1-158612511-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612511C>A , CM000663.2:g.158612511C>A	GRCh38
NC_000001.10:g.158582301C>A , CM000663.1:g.158582301C>A	GRCh37
NC_000001.9:g.156848925C>A	NCBI36
NG_011474.1:g.79206G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641002.1:c.*5131C>A (OR10Z1) MANE Select	ENSP00000493003.1:n.*5131C>A
ENST00000643759.2:c.7134+306G>T (SPTA1) MANE Select	ENSP00000495214.1:n.7134+306G>T
ENST00000368147.8:c.7134+306G>T (SPTA1)	ENSP00000357129.4:n.7134+306G>T
ENST00000614909.4:c.7134+306G>T (SPTA1)	ENSP00000482595.1:n.7134+306G>T
NM_003126.2:c.7134+306G>T (SPTA1)	NP_003117.2:n.7134+306G>T
XM_011509916.1:c.7134+306G>T (SPTA1)	XP_011508218.1:n.7134+306G>T
XM_011509917.1:c.7116+306G>T (SPTA1)	XP_011508219.1:n.7116+306G>T
NM_003126.3:c.7134+306G>T (SPTA1)	NP_003117.2:n.7134+306G>T
XM_011509916.2:c.7134+306G>T (SPTA1)	XP_011508218.1:n.7134+306G>T
XM_011509917.3:c.7116+306G>T (SPTA1)	XP_011508219.1:n.7116+306G>T
NM_003126.4:c.7134+306G>T (SPTA1) MANE Select	NP_003117.2:n.7134+306G>T
NM_001004478.2:c.*5131C>A (OR10Z1) MANE Select	NP_001004478.1:n.*5131C>A