Canonical Allele Identifier: CA951716310

Gene: TRPV4

Linked Data

• dbSNP Id: rs1889554934

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109784476A>T , CM000674.2:g.109784476A>T	GRCh38
NC_000012.11:g.110222281A>T , CM000674.1:g.110222281A>T	GRCh37
NC_000012.10:g.108706664A>T	NCBI36
NG_017090.1:g.53932T>A , LRG_372:g.53932T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.2337-39T>A MANE Select	ENSP00000261740.2:n.2337-39T>A
ENST00000418703.7:c.2337-39T>A	ENSP00000406191.2:n.2337-39T>A
ENST00000674908.1:c.*1424-39T>A	ENSP00000502012.1:n.*1424-39T>A
ENST00000675670.1:c.2337-39T>A	ENSP00000502135.1:n.2337-39T>A
ENST00000261740.6:c.2337-39T>A	ENSP00000261740.2:n.2337-39T>A
ENST00000418703.6:c.2337-39T>A	ENSP00000406191.2:n.2337-39T>A
ENST00000536838.1:c.2235-39T>A	ENSP00000444336.1:n.2235-39T>A
ENST00000537083.5:c.2157-39T>A	ENSP00000442738.1:n.2157-39T>A
ENST00000538125.5:c.*720-39T>A	ENSP00000437449.1:n.*720-39T>A
ENST00000541794.5:c.2196-39T>A	ENSP00000442167.1:n.2196-39T>A
ENST00000544971.5:c.2016-39T>A	ENSP00000443611.1:n.2016-39T>A
NM_001177428.1:c.2196-39T>A	NP_001170899.1:n.2196-39T>A
NM_001177431.1:c.2235-39T>A	NP_001170902.1:n.2235-39T>A
NM_001177433.1:c.2016-39T>A	NP_001170904.1:n.2016-39T>A
NM_021625.4:c.2337-39T>A , LRG_372t1:c.2337-39T>A	NP_067638.3:n.2337-39T>A
NM_147204.2:c.2157-39T>A	NP_671737.1:n.2157-39T>A
XM_005253918.1:c.2337-39T>A	XP_005253975.1:n.2337-39T>A
XM_011538630.1:c.2337-39T>A	XP_011536932.1:n.2337-39T>A
XM_011538631.1:c.2196-39T>A	XP_011536933.1:n.2196-39T>A
XM_011538632.1:c.2157-39T>A	XP_011536934.1:n.2157-39T>A
XM_011538633.1:c.2016-39T>A	XP_011536935.1:n.2016-39T>A
XM_011538630.2:c.2490-39T>A	XP_011536932.2:n.2490-39T>A
XM_011538631.2:c.2349-39T>A	XP_011536933.2:n.2349-39T>A
XM_011538632.2:c.2310-39T>A	XP_011536934.2:n.2310-39T>A
XM_011538633.2:c.2169-39T>A	XP_011536935.2:n.2169-39T>A
XM_017019774.1:c.2337-39T>A	XP_016875263.1:n.2337-39T>A
NM_021625.5:c.2337-39T>A MANE Select	NP_067638.3:n.2337-39T>A