Canonical Allele Identifier: CA6780252
Community Standard Title: NM_021625.5(TRPV4):c.1392C>T (p.Arg464=)
Gene: TRPV4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109794428G>A , CM000674.2:g.109794428G>A GRCh38
NC_000012.11:g.110232233G>A , CM000674.1:g.110232233G>A GRCh37
NC_000012.10:g.108716616G>A NCBI36
NG_017090.1:g.43980C>T , LRG_372:g.43980C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021625.5:c.1392C>T MANE Select NP_067638.3:p.Arg464=
ENST00000261740.7:c.1392C>T MANE Select ENSP00000261740.2:p.Arg464=
NM_001177428.1:c.1251C>T NP_001170899.1:p.Arg417=
NM_001177431.1:c.1290C>T NP_001170902.1:p.Arg430=
NM_001177433.1:c.1071C>T NP_001170904.1:p.Arg357=
NM_021625.4:c.1392C>T , LRG_372t1:c.1392C>T NP_067638.3:p.Arg464=
NM_147204.2:c.1212C>T NP_671737.1:p.Arg404=
ENST00000261740.6:c.1392C>T ENSP00000261740.2:p.Arg464=
ENST00000418703.6:c.1392C>T ENSP00000406191.2:p.Arg464=
ENST00000418703.7:c.1392C>T ENSP00000406191.2:p.Arg464=
ENST00000536838.1:c.1290C>T ENSP00000444336.1:p.Arg430=
ENST00000537083.5:c.1212C>T ENSP00000442738.1:p.Arg404=
ENST00000538125.5:c.1392C>T ENSP00000437449.1:p.Arg464=
ENST00000541794.5:c.1251C>T ENSP00000442167.1:p.Arg417=
ENST00000544971.5:c.1071C>T ENSP00000443611.1:p.Arg357=
ENST00000674908.1:c.*479C>T ENSP00000502012.1:n.*479C>T
ENST00000675533.1:n.1423C>T
ENST00000675670.1:c.1392C>T ENSP00000502135.1:p.Arg464=
ENST00000676376.1:n.1423C>T
XM_005253918.1:c.1392C>T XP_005253975.1:p.Arg464=
XM_011538630.1:c.1392C>T XP_011536932.1:p.Arg464=
XM_011538630.2:c.1545C>T XP_011536932.2:p.Arg515=
XM_011538631.1:c.1251C>T XP_011536933.1:p.Arg417=
XM_011538631.2:c.1404C>T XP_011536933.2:p.Arg468=
XM_011538632.1:c.1212C>T XP_011536934.1:p.Arg404=
XM_011538632.2:c.1365C>T XP_011536934.2:p.Arg455=
XM_011538633.1:c.1071C>T XP_011536935.1:p.Arg357=
XM_011538633.2:c.1224C>T XP_011536935.2:p.Arg408=
XM_011538634.1:c.1392C>T XP_011536936.1:p.Arg464=
XM_011538634.2:c.1545C>T XP_011536936.2:p.Arg515=
XM_011538635.1:c.1545C>T XP_011536937.1:p.Arg515=
XM_011538635.2:c.1545C>T XP_011536937.1:p.Arg515=
XM_011538636.1:c.1545C>T XP_011536938.1:p.Arg515=
XM_017019774.1:c.1392C>T XP_016875263.1:p.Arg464=