Canonical Allele Identifier: CA2687610636
Gene: TRPA1 HGNC NCBI
MSC-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72034372del , CM000670.2:g.72034372del GRCh38
NC_000008.10:g.72946607del , CM000670.1:g.72946607del GRCh37
NC_000008.9:g.73109161del NCBI36
NG_033890.1:g.46216del

Transcript Alleles

HGVS Amino-acid change
ENST00000262209.5:c.2564del (TRPA1) MANE Select ENSP00000262209.4:p.Asn855IlefsTer11
ENST00000262209.4:c.2564del (TRPA1) ENSP00000262209.4:p.Asn855IlefsTer11
ENST00000519720.5:n.660del (TRPA1)
ENST00000523582.5:c.2120del (TRPA1) ENSP00000428151.1:p.Asn707IlefsTer11
NM_007332.2:c.2564del (TRPA1) NP_015628.2:p.Asn855IlefsTer11
NR_033651.1:n.434-18167del (MSC-AS1)
NR_033652.1:n.1029-18167del (MSC-AS1)
XM_011517624.1:c.2639del (TRPA1) XP_011515926.1:p.Asn880IlefsTer11
XM_011517625.1:c.2564del (TRPA1) XP_011515927.1:p.Asn855IlefsTer11
XM_011517624.2:c.2639del (TRPA1) XP_011515926.1:p.Asn880IlefsTer11
XM_011517625.2:c.2564del (TRPA1) XP_011515927.1:p.Asn855IlefsTer11
XM_017013946.1:c.2564del (TRPA1) XP_016869435.1:p.Asn855IlefsTer11
NM_007332.3:c.2564del (TRPA1) MANE Select NP_015628.2:p.Asn855IlefsTer11