Canonical Allele Identifier: CA397692792

Gene: TRPV1

Linked Data

• MyVariant Identifiers: chr17:g.3493105A>C (hg19) ; chr17:g.3589811A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3589811A>C , CM000679.2:g.3589811A>C	GRCh38
NC_000017.10:g.3493105A>C , CM000679.1:g.3493105A>C	GRCh37
NC_000017.9:g.3439854A>C	NCBI36
NG_029716.1:g.24601T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000572705.2:c.1040T>G MANE Select	ENSP00000459962.1:p.Ile347Ser
ENST00000650505.1:c.1040T>G	ENSP00000497337.1:p.Ile347Ser
ENST00000310522.5:c.1040T>G	ENSP00000311692.5:p.Ile347Ser
ENST00000399756.8:c.1040T>G	ENSP00000382659.4:p.Ile347Ser
ENST00000399759.7:c.1040T>G	ENSP00000382661.3:p.Ile347Ser
ENST00000425167.6:c.1040T>G	ENSP00000409627.2:p.Ile347Ser
ENST00000571088.5:c.1040T>G	ENSP00000461007.1:p.Ile347Ser
ENST00000572705.1:c.1040T>G	ENSP00000459962.1:p.Ile347Ser
ENST00000572919.1:c.*2324T>G	ENSP00000461416.1:n.*2324T>G
ENST00000574085.5:n.1127T>G
ENST00000576351.5:c.1040T>G	ENSP00000459042.1:p.Ile347Ser
NM_018727.5:c.1040T>G	NP_061197.4:p.Ile347Ser
NM_080704.3:c.1040T>G	NP_542435.2:p.Ile347Ser
NM_080705.3:c.1040T>G	NP_542436.2:p.Ile347Ser
NM_080706.3:c.1040T>G	NP_542437.2:p.Ile347Ser
NM_080704.4:c.1040T>G MANE Select	NP_542435.2:p.Ile347Ser
NM_080705.4:c.1040T>G	NP_542436.2:p.Ile347Ser