Canonical Allele Identifier: CA371473514
Gene: TRPA1 HGNC NCBI
MSC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72034372T>A , CM000670.2:g.72034372T>A GRCh38
NC_000008.10:g.72946607T>A , CM000670.1:g.72946607T>A GRCh37
NC_000008.9:g.73109161T>A NCBI36
NG_033890.1:g.46213A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262209.5:c.2561A>T (TRPA1) MANE Select ENSP00000262209.4:p.Glu854Val
ENST00000262209.4:c.2561A>T (TRPA1) ENSP00000262209.4:p.Glu854Val
ENST00000519720.5:n.657A>T (TRPA1)
ENST00000523582.5:c.2117A>T (TRPA1) ENSP00000428151.1:p.Glu706Val
NM_007332.2:c.2561A>T (TRPA1) NP_015628.2:p.Glu854Val
NR_033651.1:n.434-18167T>A (MSC-AS1)
NR_033652.1:n.1029-18167T>A (MSC-AS1)
XM_011517624.1:c.2636A>T (TRPA1) XP_011515926.1:p.Glu879Val
XM_011517625.1:c.2561A>T (TRPA1) XP_011515927.1:p.Glu854Val
XM_011517624.2:c.2636A>T (TRPA1) XP_011515926.1:p.Glu879Val
XM_011517625.2:c.2561A>T (TRPA1) XP_011515927.1:p.Glu854Val
XM_017013946.1:c.2561A>T (TRPA1) XP_016869435.1:p.Glu854Val
NM_007332.3:c.2561A>T (TRPA1) MANE Select NP_015628.2:p.Glu854Val