Canonical Allele Identifier: CA2243927589
Community Standard Title: NM_080704.4(TRPV1):c.*256T=
Gene: TRPV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3566559A= , CM000679.2:g.3566559A= GRCh38
NC_000017.10:g.3469853A= , CM000679.1:g.3469853A= GRCh37
NC_000017.9:g.3416603A= NCBI36
NG_029716.1:g.47853T=

Transcript Alleles

HGVS Amino-acid Change
NM_080704.4:c.*256T= MANE Select NP_542435.2:n.*256T=
ENST00000572705.2:c.*256T= MANE Select ENSP00000459962.1:n.*256T=
NM_018727.5:c.*256T= NP_061197.4:n.*256T=
NM_080704.3:c.*256T= NP_542435.2:n.*256T=
NM_080705.3:c.*256T= NP_542436.2:n.*256T=
NM_080705.4:c.*256T= NP_542436.2:n.*256T=
NM_080706.3:c.*256T= NP_542437.2:n.*256T=
ENST00000399756.8:c.*256T= ENSP00000382659.4:n.*256T=
ENST00000399759.7:c.*256T= ENSP00000382661.3:n.*256T=
ENST00000571088.5:c.*256T= ENSP00000461007.1:n.*256T=
ENST00000572705.1:c.*256T= ENSP00000459962.1:n.*256T=
ENST00000650505.1:c.*1257T= ENSP00000497337.1:n.*1257T=