Canonical Allele Identifier: CA481867579

Gene: TRPV4

Linked Data

• MyVariant Identifiers: chr12:g.110236698C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109798893C>T , CM000674.2:g.109798893C>T	GRCh38
NC_000012.11:g.110236698C>T , CM000674.1:g.110236698C>T	GRCh37
NC_000012.10:g.108721081C>T	NCBI36
NG_017090.1:g.39515G>A , LRG_372:g.39515G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.873G>A MANE Select	ENSP00000261740.2:p.Leu291=
ENST00000418703.7:c.873G>A	ENSP00000406191.2:p.Leu291=
ENST00000674908.1:c.902G>A	ENSP00000502012.1:p.Trp301Ter
ENST00000675533.1:n.904G>A
ENST00000675670.1:c.873G>A	ENSP00000502135.1:p.Leu291=
ENST00000676376.1:n.904G>A
ENST00000261740.6:c.873G>A	ENSP00000261740.2:p.Leu291=
ENST00000418703.6:c.873G>A	ENSP00000406191.2:p.Leu291=
ENST00000536838.1:c.771G>A	ENSP00000444336.1:p.Leu257=
ENST00000537083.5:c.873G>A	ENSP00000442738.1:p.Leu291=
ENST00000538125.5:c.873G>A	ENSP00000437449.1:p.Leu291=
ENST00000541794.5:c.732G>A	ENSP00000442167.1:p.Leu244=
ENST00000544971.5:c.732G>A	ENSP00000443611.1:p.Leu244=
NM_001177428.1:c.732G>A	NP_001170899.1:p.Leu244=
NM_001177431.1:c.771G>A	NP_001170902.1:p.Leu257=
NM_001177433.1:c.732G>A	NP_001170904.1:p.Leu244=
NM_021625.4:c.873G>A , LRG_372t1:c.873G>A	NP_067638.3:p.Leu291=
NM_147204.2:c.873G>A	NP_671737.1:p.Leu291=
XM_005253918.1:c.873G>A	XP_005253975.1:p.Leu291=
XM_011538630.1:c.873G>A	XP_011536932.1:p.Leu291=
XM_011538631.1:c.732G>A	XP_011536933.1:p.Leu244=
XM_011538632.1:c.873G>A	XP_011536934.1:p.Leu291=
XM_011538633.1:c.732G>A	XP_011536935.1:p.Leu244=
XM_011538634.1:c.873G>A	XP_011536936.1:p.Leu291=
XM_011538635.1:c.1026G>A	XP_011536937.1:p.Leu342=
XM_011538636.1:c.1026G>A	XP_011536938.1:p.Leu342=
XM_011538630.2:c.1026G>A	XP_011536932.2:p.Leu342=
XM_011538631.2:c.885G>A	XP_011536933.2:p.Leu295=
XM_011538632.2:c.1026G>A	XP_011536934.2:p.Leu342=
XM_011538633.2:c.885G>A	XP_011536935.2:p.Leu295=
XM_011538634.2:c.1026G>A	XP_011536936.2:p.Leu342=
XM_011538635.2:c.1026G>A	XP_011536937.1:p.Leu342=
XM_017019774.1:c.873G>A	XP_016875263.1:p.Leu291=
NM_021625.5:c.873G>A MANE Select	NP_067638.3:p.Leu291=