Canonical Allele Identifier: CA1201536742

Gene: OR10Z1 SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612502C= , CM000663.2:g.158612502C=	GRCh38
NC_000001.10:g.158582292C= , CM000663.1:g.158582292C=	GRCh37
NC_000001.9:g.156848916C=	NCBI36
NG_011474.1:g.79215G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641002.1:c.*5122C= (OR10Z1) MANE Select	ENSP00000493003.1:n.*5122C=
ENST00000643759.2:c.7134+315G= (SPTA1) MANE Select	ENSP00000495214.1:n.7134+315G=
ENST00000368147.8:c.7134+315G= (SPTA1)	ENSP00000357129.4:n.7134+315G=
ENST00000614909.4:c.7134+315G= (SPTA1)	ENSP00000482595.1:n.7134+315G=
NM_003126.2:c.7134+315G= (SPTA1)	NP_003117.2:n.7134+315G=
XM_011509916.1:c.7134+315G= (SPTA1)	XP_011508218.1:n.7134+315G=
XM_011509917.1:c.7116+315G= (SPTA1)	XP_011508219.1:n.7116+315G=
NM_003126.3:c.7134+315G= (SPTA1)	NP_003117.2:n.7134+315G=
XM_011509916.2:c.7134+315G= (SPTA1)	XP_011508218.1:n.7134+315G=
XM_011509917.3:c.7116+315G= (SPTA1)	XP_011508219.1:n.7116+315G=
NM_003126.4:c.7134+315G= (SPTA1) MANE Select	NP_003117.2:n.7134+315G=
NM_001004478.2:c.*5122C= (OR10Z1) MANE Select	NP_001004478.1:n.*5122C=