Canonical Allele Identifier: CA31249111

Gene: OR10Z1 SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158610877A>G , CM000663.2:g.158610877A>G	GRCh38
NC_000001.10:g.158580667A>G , CM000663.1:g.158580667A>G	GRCh37
NC_000001.9:g.156847291A>G	NCBI36
NG_011474.1:g.80840T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001004478.2:c.*3497A>G (OR10Z1) MANE Select	NP_001004478.1:n.*3497A>G
NM_003126.4:c.*387T>C (SPTA1) MANE Select	NP_003117.2:n.*387T>C
ENST00000641002.1:c.*3497A>G (OR10Z1) MANE Select	ENSP00000493003.1:n.*3497A>G
ENST00000643759.2:c.*387T>C (SPTA1) MANE Select	ENSP00000495214.1:n.*387T>C
NM_003126.2:c.*387T>C (SPTA1)	NP_003117.2:n.*387T>C
NM_003126.3:c.*387T>C (SPTA1)	NP_003117.2:n.*387T>C
ENST00000368147.8:c.*387T>C (SPTA1)	ENSP00000357129.4:n.*387T>C
ENST00000614909.4:c.*353T>C (SPTA1)	ENSP00000482595.1:n.*353T>C
XM_011509916.1:c.*387T>C (SPTA1)	XP_011508218.1:n.*387T>C
XM_011509916.2:c.*387T>C (SPTA1)	XP_011508218.1:n.*387T>C
XM_011509917.1:c.*387T>C (SPTA1)	XP_011508219.1:n.*387T>C
XM_011509917.3:c.*387T>C (SPTA1)	XP_011508219.1:n.*387T>C