Canonical Allele Identifier: CA6779947

Gene: TRPV4

Linked Data

• dbSNP Id: rs763582664
• ExAC: 12:110222287 G / A
• gnomAD v2: 12-110222287-G-A
• gnomAD v3: 12-109784482-G-A
• gnomAD v4: 12-109784482-G-A
• MyVariant Identifiers: chr12:g.110222287G>A (hg19) ; chr12:g.109784482G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109784482G>A , CM000674.2:g.109784482G>A	GRCh38
NC_000012.11:g.110222287G>A , CM000674.1:g.110222287G>A	GRCh37
NC_000012.10:g.108706670G>A	NCBI36
NG_017090.1:g.53926C>T , LRG_372:g.53926C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.2337-45C>T MANE Select	ENSP00000261740.2:n.2337-45C>T
ENST00000418703.7:c.2337-45C>T	ENSP00000406191.2:n.2337-45C>T
ENST00000674908.1:c.*1424-45C>T	ENSP00000502012.1:n.*1424-45C>T
ENST00000675670.1:c.2337-45C>T	ENSP00000502135.1:n.2337-45C>T
ENST00000261740.6:c.2337-45C>T	ENSP00000261740.2:n.2337-45C>T
ENST00000418703.6:c.2337-45C>T	ENSP00000406191.2:n.2337-45C>T
ENST00000536838.1:c.2235-45C>T	ENSP00000444336.1:n.2235-45C>T
ENST00000537083.5:c.2157-45C>T	ENSP00000442738.1:n.2157-45C>T
ENST00000538125.5:c.*720-45C>T	ENSP00000437449.1:n.*720-45C>T
ENST00000541794.5:c.2196-45C>T	ENSP00000442167.1:n.2196-45C>T
ENST00000544971.5:c.2016-45C>T	ENSP00000443611.1:n.2016-45C>T
NM_001177428.1:c.2196-45C>T	NP_001170899.1:n.2196-45C>T
NM_001177431.1:c.2235-45C>T	NP_001170902.1:n.2235-45C>T
NM_001177433.1:c.2016-45C>T	NP_001170904.1:n.2016-45C>T
NM_021625.4:c.2337-45C>T , LRG_372t1:c.2337-45C>T	NP_067638.3:n.2337-45C>T
NM_147204.2:c.2157-45C>T	NP_671737.1:n.2157-45C>T
XM_005253918.1:c.2337-45C>T	XP_005253975.1:n.2337-45C>T
XM_011538630.1:c.2337-45C>T	XP_011536932.1:n.2337-45C>T
XM_011538631.1:c.2196-45C>T	XP_011536933.1:n.2196-45C>T
XM_011538632.1:c.2157-45C>T	XP_011536934.1:n.2157-45C>T
XM_011538633.1:c.2016-45C>T	XP_011536935.1:n.2016-45C>T
XM_011538630.2:c.2490-45C>T	XP_011536932.2:n.2490-45C>T
XM_011538631.2:c.2349-45C>T	XP_011536933.2:n.2349-45C>T
XM_011538632.2:c.2310-45C>T	XP_011536934.2:n.2310-45C>T
XM_011538633.2:c.2169-45C>T	XP_011536935.2:n.2169-45C>T
XM_017019774.1:c.2337-45C>T	XP_016875263.1:n.2337-45C>T
NM_021625.5:c.2337-45C>T MANE Select	NP_067638.3:n.2337-45C>T