Canonical Allele Identifier: CA6779983

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109786820C>T , CM000674.2:g.109786820C>T	GRCh38
NC_000012.11:g.110224625C>T , CM000674.1:g.110224625C>T	GRCh37
NC_000012.10:g.108709008C>T	NCBI36
NG_017090.1:g.51588G>A , LRG_372:g.51588G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.2226G>A MANE Select	ENSP00000261740.2:p.Leu742=
ENST00000418703.7:c.2226G>A	ENSP00000406191.2:p.Leu742=
ENST00000674908.1:c.*1313G>A	ENSP00000502012.1:n.*1313G>A
ENST00000675533.1:n.2316G>A
ENST00000675670.1:c.2226G>A	ENSP00000502135.1:p.Leu742=
ENST00000261740.6:c.2226G>A	ENSP00000261740.2:p.Leu742=
ENST00000418703.6:c.2226G>A	ENSP00000406191.2:p.Leu742=
ENST00000536838.1:c.2124G>A	ENSP00000444336.1:p.Leu708=
ENST00000537083.5:c.2046G>A	ENSP00000442738.1:p.Leu682=
ENST00000538125.5:c.*609G>A	ENSP00000437449.1:n.*609G>A
ENST00000541794.5:c.2085G>A	ENSP00000442167.1:p.Leu695=
ENST00000544971.5:c.1905G>A	ENSP00000443611.1:p.Leu635=
NM_001177428.1:c.2085G>A	NP_001170899.1:p.Leu695=
NM_001177431.1:c.2124G>A	NP_001170902.1:p.Leu708=
NM_001177433.1:c.1905G>A	NP_001170904.1:p.Leu635=
NM_021625.4:c.2226G>A , LRG_372t1:c.2226G>A	NP_067638.3:p.Leu742=
NM_147204.2:c.2046G>A	NP_671737.1:p.Leu682=
XM_005253918.1:c.2226G>A	XP_005253975.1:p.Leu742=
XM_011538630.1:c.2226G>A	XP_011536932.1:p.Leu742=
XM_011538631.1:c.2085G>A	XP_011536933.1:p.Leu695=
XM_011538632.1:c.2046G>A	XP_011536934.1:p.Leu682=
XM_011538633.1:c.1905G>A	XP_011536935.1:p.Leu635=
XM_011538634.1:c.*56G>A	XP_011536936.1:n.*56G>A
XM_011538630.2:c.2379G>A	XP_011536932.2:p.Leu793=
XM_011538631.2:c.2238G>A	XP_011536933.2:p.Leu746=
XM_011538632.2:c.2199G>A	XP_011536934.2:p.Leu733=
XM_011538633.2:c.2058G>A	XP_011536935.2:p.Leu686=
XM_011538634.2:c.*56G>A	XP_011536936.2:n.*56G>A
XM_017019774.1:c.2226G>A	XP_016875263.1:p.Leu742=
NM_021625.5:c.2226G>A MANE Select	NP_067638.3:p.Leu742=