Canonical Allele Identifier: CA1232143479

Gene: OR2C3 GCSAML GCSAML-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.247526230C>A , CM000663.2:g.247526230C>A	GRCh38
NC_000001.10:g.247689532C>A , CM000663.1:g.247689532C>A	GRCh37
NC_000001.9:g.245756155C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366487.4:c.*5319G>T (OR2C3)	ENSP00000355443.3:n.*5319G>T
ENST00000641802.1:c.*5319G>T (OR2C3) MANE Select	ENSP00000493385.1:n.*5319G>T
ENST00000673193.1:n.658+140G>T (OR2C3)
ENST00000366489.5:c.-262-710C>A (GCSAML)	ENSP00000355445.1:n.-262-710C>A
ENST00000366491.6:c.-378-710C>A (GCSAML)	ENSP00000355447.2:n.-378-710C>A
ENST00000463359.5:c.-68+7622C>A (GCSAML)	ENSP00000434526.1:n.-68+7622C>A
ENST00000526896.5:c.-171-710C>A (GCSAML)	ENSP00000436079.1:n.-171-710C>A
ENST00000527084.5:c.-182-710C>A (GCSAML)	ENSP00000432118.1:n.-182-710C>A
ENST00000527541.5:c.-122-710C>A (GCSAML)	ENSP00000435110.1:n.-122-710C>A
ENST00000529512.5:c.-182-710C>A (GCSAML)	ENSP00000434084.1:n.-182-710C>A
ENST00000531662.1:n.369-710C>A (GCSAML)
ENST00000536561.5:c.-171-710C>A (GCSAML)	ENSP00000446460.2:n.-171-710C>A
ENST00000623578.3:c.-182-710C>A (GCSAML)	ENSP00000485175.1:n.-182-710C>A
NM_001281834.1:c.-378-710C>A (GCSAML)	NP_001268763.1:n.-378-710C>A
NM_001281835.1:c.-262-710C>A (GCSAML)	NP_001268764.1:n.-262-710C>A
NM_001281836.1:c.-182-710C>A (GCSAML)	NP_001268765.1:n.-182-710C>A
NM_001281837.1:c.-182-710C>A (GCSAML)	NP_001268766.1:n.-182-710C>A
NM_001281838.1:c.-122-710C>A (GCSAML)	NP_001268767.1:n.-122-710C>A
NM_001281853.1:c.-171-710C>A (GCSAML)	NP_001268782.1:n.-171-710C>A
NR_027309.2:n.658+140G>T (GCSAML-AS1)
XM_011544098.1:c.29-710C>A (GCSAML)	XP_011542400.1:n.29-710C>A
XM_011544099.1:c.-262-710C>A (GCSAML)	XP_011542401.1:n.-262-710C>A
XM_011544100.1:c.-16-710C>A (GCSAML)	XP_011542402.1:n.-16-710C>A
XM_024453417.1:c.-263+259C>A (GCSAML)	XP_024309185.1:n.-263+259C>A
NM_001281834.2:c.-378-710C>A (GCSAML)	NP_001268763.1:n.-378-710C>A
NM_001281835.2:c.-262-710C>A (GCSAML)	NP_001268764.1:n.-262-710C>A
NM_001281836.2:c.-182-710C>A (GCSAML)	NP_001268765.1:n.-182-710C>A
NM_001281838.2:c.-122-710C>A (GCSAML)	NP_001268767.1:n.-122-710C>A
NM_198074.6:c.*5319G>T (OR2C3) MANE Select	NP_932340.4:n.*5319G>T