Canonical Allele Identifier: CA2062573102

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109798817G= , CM000674.2:g.109798817G=	GRCh38
NC_000012.11:g.110236622G= , CM000674.1:g.110236622G=	GRCh37
NC_000012.10:g.108721005G=	NCBI36
NG_017090.1:g.39591C= , LRG_372:g.39591C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.949C= MANE Select	ENSP00000261740.2:p.Gln317=
ENST00000418703.7:c.949C=	ENSP00000406191.2:p.Gln317=
ENST00000674908.1:c.*36C=	ENSP00000502012.1:n.*36C=
ENST00000675533.1:n.980C=
ENST00000675670.1:c.949C=	ENSP00000502135.1:p.Gln317=
ENST00000676376.1:n.980C=
ENST00000261740.6:c.949C=	ENSP00000261740.2:p.Gln317=
ENST00000418703.6:c.949C=	ENSP00000406191.2:p.Gln317=
ENST00000536838.1:c.847C=	ENSP00000444336.1:p.Gln283=
ENST00000537083.5:c.949C=	ENSP00000442738.1:p.Gln317=
ENST00000538125.5:c.949C=	ENSP00000437449.1:p.Gln317=
ENST00000541794.5:c.808C=	ENSP00000442167.1:p.Gln270=
ENST00000544971.5:c.808C=	ENSP00000443611.1:p.Gln270=
NM_001177428.1:c.808C=	NP_001170899.1:p.Gln270=
NM_001177431.1:c.847C=	NP_001170902.1:p.Gln283=
NM_001177433.1:c.808C=	NP_001170904.1:p.Gln270=
NM_021625.4:c.949C= , LRG_372t1:c.949C=	NP_067638.3:p.Gln317=
NM_147204.2:c.949C=	NP_671737.1:p.Gln317=
XM_005253918.1:c.949C=	XP_005253975.1:p.Gln317=
XM_011538630.1:c.949C=	XP_011536932.1:p.Gln317=
XM_011538631.1:c.808C=	XP_011536933.1:p.Gln270=
XM_011538632.1:c.949C=	XP_011536934.1:p.Gln317=
XM_011538633.1:c.808C=	XP_011536935.1:p.Gln270=
XM_011538634.1:c.949C=	XP_011536936.1:p.Gln317=
XM_011538635.1:c.1102C=	XP_011536937.1:p.Gln368=
XM_011538636.1:c.1102C=	XP_011536938.1:p.Gln368=
XM_011538630.2:c.1102C=	XP_011536932.2:p.Gln368=
XM_011538631.2:c.961C=	XP_011536933.2:p.Gln321=
XM_011538632.2:c.1102C=	XP_011536934.2:p.Gln368=
XM_011538633.2:c.961C=	XP_011536935.2:p.Gln321=
XM_011538634.2:c.1102C=	XP_011536936.2:p.Gln368=
XM_011538635.2:c.1102C=	XP_011536937.1:p.Gln368=
XM_017019774.1:c.949C=	XP_016875263.1:p.Gln317=
NM_021625.5:c.949C= MANE Select	NP_067638.3:p.Gln317=