Canonical Allele Identifier: CA4780462

Gene: TRPA1 MSC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72034375A>C , CM000670.2:g.72034375A>C	GRCh38
NC_000008.10:g.72946610A>C , CM000670.1:g.72946610A>C	GRCh37
NC_000008.9:g.73109164A>C	NCBI36
NG_033890.1:g.46210T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007332.3:c.2558T>G (TRPA1) MANE Select	NP_015628.2:p.Phe853Cys
ENST00000262209.5:c.2558T>G (TRPA1) MANE Select	ENSP00000262209.4:p.Phe853Cys
NM_007332.2:c.2558T>G (TRPA1)	NP_015628.2:p.Phe853Cys
NR_033651.1:n.434-18164A>C (MSC-AS1)
NR_033652.1:n.1029-18164A>C (MSC-AS1)
ENST00000262209.4:c.2558T>G (TRPA1)	ENSP00000262209.4:p.Phe853Cys
ENST00000519720.5:n.654T>G (TRPA1)
ENST00000523582.5:c.2114T>G (TRPA1)	ENSP00000428151.1:p.Phe705Cys
XM_011517624.1:c.2633T>G (TRPA1)	XP_011515926.1:p.Phe878Cys
XM_011517624.2:c.2633T>G (TRPA1)	XP_011515926.1:p.Phe878Cys
XM_011517625.1:c.2558T>G (TRPA1)	XP_011515927.1:p.Phe853Cys
XM_011517625.2:c.2558T>G (TRPA1)	XP_011515927.1:p.Phe853Cys
XM_017013946.1:c.2558T>G (TRPA1)	XP_016869435.1:p.Phe853Cys