Canonical Allele Identifier: CA889965448

Gene: OR10Z1 SPTA1

Linked Data

• dbSNP Id: rs1303445850
• gnomAD v3: 1-158612500-C-T
• gnomAD v4: 1-158612500-C-T
• MyVariant Identifiers: chr1:g.158582290C>T (hg19) ; chr1:g.158612500C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612500C>T , CM000663.2:g.158612500C>T	GRCh38
NC_000001.10:g.158582290C>T , CM000663.1:g.158582290C>T	GRCh37
NC_000001.9:g.156848914C>T	NCBI36
NG_011474.1:g.79217G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641002.1:c.*5120C>T (OR10Z1) MANE Select	ENSP00000493003.1:n.*5120C>T
ENST00000643759.2:c.7134+317G>A (SPTA1) MANE Select	ENSP00000495214.1:n.7134+317G>A
ENST00000368147.8:c.7134+317G>A (SPTA1)	ENSP00000357129.4:n.7134+317G>A
ENST00000614909.4:c.7134+317G>A (SPTA1)	ENSP00000482595.1:n.7134+317G>A
NM_003126.2:c.7134+317G>A (SPTA1)	NP_003117.2:n.7134+317G>A
XM_011509916.1:c.7134+317G>A (SPTA1)	XP_011508218.1:n.7134+317G>A
XM_011509917.1:c.7116+317G>A (SPTA1)	XP_011508219.1:n.7116+317G>A
NM_003126.3:c.7134+317G>A (SPTA1)	NP_003117.2:n.7134+317G>A
XM_011509916.2:c.7134+317G>A (SPTA1)	XP_011508218.1:n.7134+317G>A
XM_011509917.3:c.7116+317G>A (SPTA1)	XP_011508219.1:n.7116+317G>A
NM_003126.4:c.7134+317G>A (SPTA1) MANE Select	NP_003117.2:n.7134+317G>A
NM_001004478.2:c.*5120C>T (OR10Z1) MANE Select	NP_001004478.1:n.*5120C>T