Canonical Allele Identifier: CA2062564564

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109792678C= , CM000674.2:g.109792678C=	GRCh38
NC_000012.11:g.110230483C= , CM000674.1:g.110230483C=	GRCh37
NC_000012.10:g.108714866C=	NCBI36
NG_017090.1:g.45730G= , LRG_372:g.45730G=

Transcript Alleles

HGVS	Amino-acid Change
NM_021625.5:c.1798G= MANE Select	NP_067638.3:p.Gly600=
ENST00000261740.7:c.1798G= MANE Select	ENSP00000261740.2:p.Gly600=
NM_001177428.1:c.1657G=	NP_001170899.1:p.Gly553=
NM_001177431.1:c.1696G=	NP_001170902.1:p.Gly566=
NM_001177433.1:c.1477G=	NP_001170904.1:p.Gly493=
NM_021625.4:c.1798G= , LRG_372t1:c.1798G=	NP_067638.3:p.Gly600=
NM_147204.2:c.1618G=	NP_671737.1:p.Gly540=
ENST00000261740.6:c.1798G=	ENSP00000261740.2:p.Gly600=
ENST00000418703.6:c.1798G=	ENSP00000406191.2:p.Gly600=
ENST00000418703.7:c.1798G=	ENSP00000406191.2:p.Gly600=
ENST00000536838.1:c.1696G=	ENSP00000444336.1:p.Gly566=
ENST00000537083.5:c.1618G=	ENSP00000442738.1:p.Gly540=
ENST00000538125.5:c.*181G=	ENSP00000437449.1:n.*181G=
ENST00000541794.5:c.1657G=	ENSP00000442167.1:p.Gly553=
ENST00000544971.5:c.1477G=	ENSP00000443611.1:p.Gly493=
ENST00000674908.1:c.*885G=	ENSP00000502012.1:n.*885G=
ENST00000675533.1:n.1829G=
ENST00000675670.1:c.1798G=	ENSP00000502135.1:p.Gly600=
ENST00000676376.1:n.1829G=
XM_005253918.1:c.1798G=	XP_005253975.1:p.Gly600=
XM_011538630.1:c.1798G=	XP_011536932.1:p.Gly600=
XM_011538630.2:c.1951G=	XP_011536932.2:p.Gly651=
XM_011538631.1:c.1657G=	XP_011536933.1:p.Gly553=
XM_011538631.2:c.1810G=	XP_011536933.2:p.Gly604=
XM_011538632.1:c.1618G=	XP_011536934.1:p.Gly540=
XM_011538632.2:c.1771G=	XP_011536934.2:p.Gly591=
XM_011538633.1:c.1477G=	XP_011536935.1:p.Gly493=
XM_011538633.2:c.1630G=	XP_011536935.2:p.Gly544=
XM_011538634.1:c.1798G=	XP_011536936.1:p.Gly600=
XM_011538634.2:c.1951G=	XP_011536936.2:p.Gly651=
XM_011538635.1:c.1951G=	XP_011536937.1:p.Gly651=
XM_011538635.2:c.1951G=	XP_011536937.1:p.Gly651=
XM_017019774.1:c.1798G=	XP_016875263.1:p.Gly600=