Canonical Allele Identifier: CA2648555318

Gene: OR10Z1 SPTA1

Linked Data

• gnomAD v4: 1-158612469-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612469G>T , CM000663.2:g.158612469G>T	GRCh38
NC_000001.10:g.158582259G>T , CM000663.1:g.158582259G>T	GRCh37
NC_000001.9:g.156848883G>T	NCBI36
NG_011474.1:g.79248C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641002.1:c.*5089G>T (OR10Z1) MANE Select	ENSP00000493003.1:n.*5089G>T
ENST00000643759.2:c.7134+348C>A (SPTA1) MANE Select	ENSP00000495214.1:n.7134+348C>A
ENST00000368147.8:c.7134+348C>A (SPTA1)	ENSP00000357129.4:n.7134+348C>A
ENST00000614909.4:c.7134+348C>A (SPTA1)	ENSP00000482595.1:n.7134+348C>A
NM_003126.2:c.7134+348C>A (SPTA1)	NP_003117.2:n.7134+348C>A
XM_011509916.1:c.7134+348C>A (SPTA1)	XP_011508218.1:n.7134+348C>A
XM_011509917.1:c.7116+348C>A (SPTA1)	XP_011508219.1:n.7116+348C>A
NM_003126.3:c.7134+348C>A (SPTA1)	NP_003117.2:n.7134+348C>A
XM_011509916.2:c.7134+348C>A (SPTA1)	XP_011508218.1:n.7134+348C>A
XM_011509917.3:c.7116+348C>A (SPTA1)	XP_011508219.1:n.7116+348C>A
NM_003126.4:c.7134+348C>A (SPTA1) MANE Select	NP_003117.2:n.7134+348C>A
NM_001004478.2:c.*5089G>T (OR10Z1) MANE Select	NP_001004478.1:n.*5089G>T