Canonical Allele Identifier: CA2062573027

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109798768T= , CM000674.2:g.109798768T=	GRCh38
NC_000012.11:g.110236573T= , CM000674.1:g.110236573T=	GRCh37
NC_000012.10:g.108720956T=	NCBI36
NG_017090.1:g.39640A= , LRG_372:g.39640A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.998A= MANE Select	ENSP00000261740.2:p.Asp333=
ENST00000418703.7:c.998A=	ENSP00000406191.2:p.Asp333=
ENST00000674908.1:c.*85A=	ENSP00000502012.1:n.*85A=
ENST00000675533.1:n.1029A=
ENST00000675670.1:c.998A=	ENSP00000502135.1:p.Asp333=
ENST00000676376.1:n.1029A=
ENST00000261740.6:c.998A=	ENSP00000261740.2:p.Asp333=
ENST00000418703.6:c.998A=	ENSP00000406191.2:p.Asp333=
ENST00000536838.1:c.896A=	ENSP00000444336.1:p.Asp299=
ENST00000537083.5:c.998A=	ENSP00000442738.1:p.Asp333=
ENST00000538125.5:c.998A=	ENSP00000437449.1:p.Asp333=
ENST00000541794.5:c.857A=	ENSP00000442167.1:p.Asp286=
ENST00000544971.5:c.857A=	ENSP00000443611.1:p.Asp286=
NM_001177428.1:c.857A=	NP_001170899.1:p.Asp286=
NM_001177431.1:c.896A=	NP_001170902.1:p.Asp299=
NM_001177433.1:c.857A=	NP_001170904.1:p.Asp286=
NM_021625.4:c.998A= , LRG_372t1:c.998A=	NP_067638.3:p.Asp333=
NM_147204.2:c.998A=	NP_671737.1:p.Asp333=
XM_005253918.1:c.998A=	XP_005253975.1:p.Asp333=
XM_011538630.1:c.998A=	XP_011536932.1:p.Asp333=
XM_011538631.1:c.857A=	XP_011536933.1:p.Asp286=
XM_011538632.1:c.998A=	XP_011536934.1:p.Asp333=
XM_011538633.1:c.857A=	XP_011536935.1:p.Asp286=
XM_011538634.1:c.998A=	XP_011536936.1:p.Asp333=
XM_011538635.1:c.1151A=	XP_011536937.1:p.Asp384=
XM_011538636.1:c.1151A=	XP_011536938.1:p.Asp384=
XM_011538630.2:c.1151A=	XP_011536932.2:p.Asp384=
XM_011538631.2:c.1010A=	XP_011536933.2:p.Asp337=
XM_011538632.2:c.1151A=	XP_011536934.2:p.Asp384=
XM_011538633.2:c.1010A=	XP_011536935.2:p.Asp337=
XM_011538634.2:c.1151A=	XP_011536936.2:p.Asp384=
XM_011538635.2:c.1151A=	XP_011536937.1:p.Asp384=
XM_017019774.1:c.998A=	XP_016875263.1:p.Asp333=
NM_021625.5:c.998A= MANE Select	NP_067638.3:p.Asp333=