Canonical Allele Identifier: CA2062572817

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109798648G= , CM000674.2:g.109798648G=	GRCh38
NC_000012.11:g.110236453G= , CM000674.1:g.110236453G=	GRCh37
NC_000012.10:g.108720836G=	NCBI36
NG_017090.1:g.39760C= , LRG_372:g.39760C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.1118C= MANE Select	ENSP00000261740.2:p.Pro373=
ENST00000418703.7:c.1118C=	ENSP00000406191.2:p.Pro373=
ENST00000674908.1:c.*205C=	ENSP00000502012.1:n.*205C=
ENST00000675533.1:n.1149C=
ENST00000675670.1:c.1118C=	ENSP00000502135.1:p.Pro373=
ENST00000676376.1:n.1149C=
ENST00000261740.6:c.1118C=	ENSP00000261740.2:p.Pro373=
ENST00000418703.6:c.1118C=	ENSP00000406191.2:p.Pro373=
ENST00000536838.1:c.1016C=	ENSP00000444336.1:p.Pro339=
ENST00000537083.5:c.1118C=	ENSP00000442738.1:p.Pro373=
ENST00000538125.5:c.1118C=	ENSP00000437449.1:p.Pro373=
ENST00000541794.5:c.977C=	ENSP00000442167.1:p.Pro326=
ENST00000544971.5:c.977C=	ENSP00000443611.1:p.Pro326=
NM_001177428.1:c.977C=	NP_001170899.1:p.Pro326=
NM_001177431.1:c.1016C=	NP_001170902.1:p.Pro339=
NM_001177433.1:c.977C=	NP_001170904.1:p.Pro326=
NM_021625.4:c.1118C= , LRG_372t1:c.1118C=	NP_067638.3:p.Pro373=
NM_147204.2:c.1118C=	NP_671737.1:p.Pro373=
XM_005253918.1:c.1118C=	XP_005253975.1:p.Pro373=
XM_011538630.1:c.1118C=	XP_011536932.1:p.Pro373=
XM_011538631.1:c.977C=	XP_011536933.1:p.Pro326=
XM_011538632.1:c.1118C=	XP_011536934.1:p.Pro373=
XM_011538633.1:c.977C=	XP_011536935.1:p.Pro326=
XM_011538634.1:c.1118C=	XP_011536936.1:p.Pro373=
XM_011538635.1:c.1271C=	XP_011536937.1:p.Pro424=
XM_011538636.1:c.1271C=	XP_011536938.1:p.Pro424=
XM_011538630.2:c.1271C=	XP_011536932.2:p.Pro424=
XM_011538631.2:c.1130C=	XP_011536933.2:p.Pro377=
XM_011538632.2:c.1271C=	XP_011536934.2:p.Pro424=
XM_011538633.2:c.1130C=	XP_011536935.2:p.Pro377=
XM_011538634.2:c.1271C=	XP_011536936.2:p.Pro424=
XM_011538635.2:c.1271C=	XP_011536937.1:p.Pro424=
XM_017019774.1:c.1118C=	XP_016875263.1:p.Pro373=
NM_021625.5:c.1118C= MANE Select	NP_067638.3:p.Pro373=