Canonical Allele Identifier: CA2062571040
Gene: TRPV4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109796642C= , CM000674.2:g.109796642C= GRCh38
NC_000012.11:g.110234447C= , CM000674.1:g.110234447C= GRCh37
NC_000012.10:g.108718830C= NCBI36
NG_017090.1:g.41766G= , LRG_372:g.41766G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261740.7:c.1215G= MANE Select ENSP00000261740.2:p.Lys405=
ENST00000418703.7:c.1215G= ENSP00000406191.2:p.Lys405=
ENST00000674908.1:c.*302G= ENSP00000502012.1:n.*302G=
ENST00000675533.1:n.1246G=
ENST00000675670.1:c.1215G= ENSP00000502135.1:p.Lys405=
ENST00000676376.1:n.1246G=
ENST00000261740.6:c.1215G= ENSP00000261740.2:p.Lys405=
ENST00000418703.6:c.1215G= ENSP00000406191.2:p.Lys405=
ENST00000536838.1:c.1113G= ENSP00000444336.1:p.Lys371=
ENST00000537083.5:c.1152+1972G= ENSP00000442738.1:n.1152+1972G=
ENST00000538125.5:c.1215G= ENSP00000437449.1:p.Lys405=
ENST00000541794.5:c.1074G= ENSP00000442167.1:p.Lys358=
ENST00000544971.5:c.1011+1972G= ENSP00000443611.1:n.1011+1972G=
NM_001177428.1:c.1074G= NP_001170899.1:p.Lys358=
NM_001177431.1:c.1113G= NP_001170902.1:p.Lys371=
NM_001177433.1:c.1011+1972G= NP_001170904.1:n.1011+1972G=
NM_021625.4:c.1215G= , LRG_372t1:c.1215G= NP_067638.3:p.Lys405=
NM_147204.2:c.1152+1972G= NP_671737.1:n.1152+1972G=
XM_005253918.1:c.1215G= XP_005253975.1:p.Lys405=
XM_011538630.1:c.1215G= XP_011536932.1:p.Lys405=
XM_011538631.1:c.1074G= XP_011536933.1:p.Lys358=
XM_011538632.1:c.1152+1972G= XP_011536934.1:n.1152+1972G=
XM_011538633.1:c.1011+1972G= XP_011536935.1:n.1011+1972G=
XM_011538634.1:c.1215G= XP_011536936.1:p.Lys405=
XM_011538635.1:c.1368G= XP_011536937.1:p.Lys456=
XM_011538636.1:c.1368G= XP_011536938.1:p.Lys456=
XM_011538630.2:c.1368G= XP_011536932.2:p.Lys456=
XM_011538631.2:c.1227G= XP_011536933.2:p.Lys409=
XM_011538632.2:c.1305+1972G= XP_011536934.2:n.1305+1972G=
XM_011538633.2:c.1164+1972G= XP_011536935.2:n.1164+1972G=
XM_011538634.2:c.1368G= XP_011536936.2:p.Lys456=
XM_011538635.2:c.1368G= XP_011536937.1:p.Lys456=
XM_017019774.1:c.1215G= XP_016875263.1:p.Lys405=
NM_021625.5:c.1215G= MANE Select NP_067638.3:p.Lys405=