Canonical Allele Identifier: CA461333773
Community Standard Title: NM_007332.3(TRPA1):c.2814T>C (p.Phe938=)
Gene: TRPA1 HGNC NCBI
MSC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72033698A>G , CM000670.2:g.72033698A>G GRCh38
NC_000008.10:g.72945933A>G , CM000670.1:g.72945933A>G GRCh37
NC_000008.9:g.73108487A>G NCBI36
NG_033890.1:g.46887T>C

Transcript Alleles

HGVS Amino-acid Change
NM_007332.3:c.2814T>C (TRPA1) MANE Select NP_015628.2:p.Phe938=
ENST00000262209.5:c.2814T>C (TRPA1) MANE Select ENSP00000262209.4:p.Phe938=
NM_007332.2:c.2814T>C (TRPA1) NP_015628.2:p.Phe938=
NR_033651.1:n.434-18841A>G (MSC-AS1)
NR_033652.1:n.1029-18841A>G (MSC-AS1)
ENST00000262209.4:c.2814T>C (TRPA1) ENSP00000262209.4:p.Phe938=
ENST00000523582.5:c.2370T>C (TRPA1) ENSP00000428151.1:p.Phe790=
XM_011517624.1:c.2889T>C (TRPA1) XP_011515926.1:p.Phe963=
XM_011517624.2:c.2889T>C (TRPA1) XP_011515926.1:p.Phe963=
XM_011517625.1:c.2814T>C (TRPA1) XP_011515927.1:p.Phe938=
XM_011517625.2:c.2814T>C (TRPA1) XP_011515927.1:p.Phe938=
XM_017013946.1:c.2814T>C (TRPA1) XP_016869435.1:p.Phe938=