Canonical Allele Identifier: CA371473522

Gene: TRPA1 MSC-AS1

Linked Data

• gnomAD v4: 8-72034375-A-G
• MyVariant Identifiers: chr8:g.72946610A>G (hg19) ; chr8:g.72034375A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000262209.5:c.2558T>C (TRPA1) MANE Select	ENSP00000262209.4:p.Phe853Ser
ENST00000262209.4:c.2558T>C (TRPA1)	ENSP00000262209.4:p.Phe853Ser
ENST00000519720.5:n.654T>C (TRPA1)
ENST00000523582.5:c.2114T>C (TRPA1)	ENSP00000428151.1:p.Phe705Ser
NM_007332.2:c.2558T>C (TRPA1)	NP_015628.2:p.Phe853Ser
NR_033651.1:n.434-18164A>G (MSC-AS1)
NR_033652.1:n.1029-18164A>G (MSC-AS1)
XM_011517624.1:c.2633T>C (TRPA1)	XP_011515926.1:p.Phe878Ser
XM_011517625.1:c.2558T>C (TRPA1)	XP_011515927.1:p.Phe853Ser
XM_011517624.2:c.2633T>C (TRPA1)	XP_011515926.1:p.Phe878Ser
XM_011517625.2:c.2558T>C (TRPA1)	XP_011515927.1:p.Phe853Ser
XM_017013946.1:c.2558T>C (TRPA1)	XP_016869435.1:p.Phe853Ser
NM_007332.3:c.2558T>C (TRPA1) MANE Select	NP_015628.2:p.Phe853Ser