Canonical Allele Identifier: CA6780357

Gene: TRPV4

Linked Data

• ClinVar Variation Id: 536873
• ClinVar RCV Id: RCV000645562 ; RCV001110539 ; RCV001112511 ; RCV001112513 ; RCV001110538 ; RCV001112512 ; RCV002422339
• dbSNP Id: rs140040335
• ExAC: 12:110236497 G / A
• gnomAD v2: 12-110236497-G-A
• gnomAD v3: 12-109798692-G-A
• gnomAD v4: 12-109798692-G-A
• MyVariant Identifiers: chr12:g.110236497G>A (hg19) ; chr12:g.109798692G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109798692G>A , CM000674.2:g.109798692G>A	GRCh38
NC_000012.11:g.110236497G>A , CM000674.1:g.110236497G>A	GRCh37
NC_000012.10:g.108720880G>A	NCBI36
NG_017090.1:g.39716C>T , LRG_372:g.39716C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.1074C>T MANE Select	ENSP00000261740.2:p.Pro358=
ENST00000418703.7:c.1074C>T	ENSP00000406191.2:p.Pro358=
ENST00000674908.1:c.*161C>T	ENSP00000502012.1:n.*161C>T
ENST00000675533.1:n.1105C>T
ENST00000675670.1:c.1074C>T	ENSP00000502135.1:p.Pro358=
ENST00000676376.1:n.1105C>T
ENST00000261740.6:c.1074C>T	ENSP00000261740.2:p.Pro358=
ENST00000418703.6:c.1074C>T	ENSP00000406191.2:p.Pro358=
ENST00000536838.1:c.972C>T	ENSP00000444336.1:p.Pro324=
ENST00000537083.5:c.1074C>T	ENSP00000442738.1:p.Pro358=
ENST00000538125.5:c.1074C>T	ENSP00000437449.1:p.Pro358=
ENST00000541794.5:c.933C>T	ENSP00000442167.1:p.Pro311=
ENST00000544971.5:c.933C>T	ENSP00000443611.1:p.Pro311=
NM_001177428.1:c.933C>T	NP_001170899.1:p.Pro311=
NM_001177431.1:c.972C>T	NP_001170902.1:p.Pro324=
NM_001177433.1:c.933C>T	NP_001170904.1:p.Pro311=
NM_021625.4:c.1074C>T , LRG_372t1:c.1074C>T	NP_067638.3:p.Pro358=
NM_147204.2:c.1074C>T	NP_671737.1:p.Pro358=
XM_005253918.1:c.1074C>T	XP_005253975.1:p.Pro358=
XM_011538630.1:c.1074C>T	XP_011536932.1:p.Pro358=
XM_011538631.1:c.933C>T	XP_011536933.1:p.Pro311=
XM_011538632.1:c.1074C>T	XP_011536934.1:p.Pro358=
XM_011538633.1:c.933C>T	XP_011536935.1:p.Pro311=
XM_011538634.1:c.1074C>T	XP_011536936.1:p.Pro358=
XM_011538635.1:c.1227C>T	XP_011536937.1:p.Pro409=
XM_011538636.1:c.1227C>T	XP_011536938.1:p.Pro409=
XM_011538630.2:c.1227C>T	XP_011536932.2:p.Pro409=
XM_011538631.2:c.1086C>T	XP_011536933.2:p.Pro362=
XM_011538632.2:c.1227C>T	XP_011536934.2:p.Pro409=
XM_011538633.2:c.1086C>T	XP_011536935.2:p.Pro362=
XM_011538634.2:c.1227C>T	XP_011536936.2:p.Pro409=
XM_011538635.2:c.1227C>T	XP_011536937.1:p.Pro409=
XM_017019774.1:c.1074C>T	XP_016875263.1:p.Pro358=
NM_021625.5:c.1074C>T MANE Select	NP_067638.3:p.Pro358=