Canonical Allele Identifier: CA6779924

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109784335G>A , CM000674.2:g.109784335G>A	GRCh38
NC_000012.11:g.110222140G>A , CM000674.1:g.110222140G>A	GRCh37
NC_000012.10:g.108706523G>A	NCBI36
NG_017090.1:g.54073C>T , LRG_372:g.54073C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021625.5:c.2439C>T MANE Select	NP_067638.3:p.Thr813=
ENST00000261740.7:c.2439C>T MANE Select	ENSP00000261740.2:p.Thr813=
NM_001177428.1:c.2298C>T	NP_001170899.1:p.Thr766=
NM_001177431.1:c.2337C>T	NP_001170902.1:p.Thr779=
NM_001177433.1:c.2118C>T	NP_001170904.1:p.Thr706=
NM_021625.4:c.2439C>T , LRG_372t1:c.2439C>T	NP_067638.3:p.Thr813=
NM_147204.2:c.2259C>T	NP_671737.1:p.Thr753=
ENST00000261740.6:c.2439C>T	ENSP00000261740.2:p.Thr813=
ENST00000418703.6:c.2439C>T	ENSP00000406191.2:p.Thr813=
ENST00000418703.7:c.2439C>T	ENSP00000406191.2:p.Thr813=
ENST00000536838.1:c.2337C>T	ENSP00000444336.1:p.Thr779=
ENST00000537083.5:c.2259C>T	ENSP00000442738.1:p.Thr753=
ENST00000538125.5:c.*822C>T	ENSP00000437449.1:n.*822C>T
ENST00000541794.5:c.2298C>T	ENSP00000442167.1:p.Thr766=
ENST00000544971.5:c.2118C>T	ENSP00000443611.1:p.Thr706=
ENST00000674908.1:c.*1526C>T	ENSP00000502012.1:n.*1526C>T
ENST00000675670.1:c.2439C>T	ENSP00000502135.1:p.Thr813=
XM_005253918.1:c.2439C>T	XP_005253975.1:p.Thr813=
XM_011538630.1:c.2439C>T	XP_011536932.1:p.Thr813=
XM_011538630.2:c.2592C>T	XP_011536932.2:p.Thr864=
XM_011538631.1:c.2298C>T	XP_011536933.1:p.Thr766=
XM_011538631.2:c.2451C>T	XP_011536933.2:p.Thr817=
XM_011538632.1:c.2259C>T	XP_011536934.1:p.Thr753=
XM_011538632.2:c.2412C>T	XP_011536934.2:p.Thr804=
XM_011538633.1:c.2118C>T	XP_011536935.1:p.Thr706=
XM_011538633.2:c.2271C>T	XP_011536935.2:p.Thr757=
XM_017019774.1:c.2439C>T	XP_016875263.1:p.Thr813=