Canonical Allele Identifier: CA2062557408
Gene: TRPV4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109783766G= , CM000674.2:g.109783766G= GRCh38
NC_000012.11:g.110221571G= , CM000674.1:g.110221571G= GRCh37
NC_000012.10:g.108705954G= NCBI36
NG_017090.1:g.54642C= , LRG_372:g.54642C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261740.7:c.2471C= MANE Select ENSP00000261740.2:p.Ser824=
ENST00000418703.7:c.2471C= ENSP00000406191.2:p.Ser824=
ENST00000674908.1:c.*1558C= ENSP00000502012.1:n.*1558C=
ENST00000675670.1:c.2471C= ENSP00000502135.1:p.Ser824=
ENST00000261740.6:c.2471C= ENSP00000261740.2:p.Ser824=
ENST00000418703.6:c.2471C= ENSP00000406191.2:p.Ser824=
ENST00000536838.1:c.2369C= ENSP00000444336.1:p.Ser790=
ENST00000537083.5:c.2291C= ENSP00000442738.1:p.Ser764=
ENST00000538125.5:c.*854C= ENSP00000437449.1:n.*854C=
ENST00000541794.5:c.2330C= ENSP00000442167.1:p.Ser777=
ENST00000544971.5:c.2150C= ENSP00000443611.1:p.Ser717=
NM_001177428.1:c.2330C= NP_001170899.1:p.Ser777=
NM_001177431.1:c.2369C= NP_001170902.1:p.Ser790=
NM_001177433.1:c.2150C= NP_001170904.1:p.Ser717=
NM_021625.4:c.2471C= , LRG_372t1:c.2471C= NP_067638.3:p.Ser824=
NM_147204.2:c.2291C= NP_671737.1:p.Ser764=
XM_005253918.1:c.2471C= XP_005253975.1:p.Ser824=
XM_011538630.1:c.2471C= XP_011536932.1:p.Ser824=
XM_011538631.1:c.2330C= XP_011536933.1:p.Ser777=
XM_011538632.1:c.2291C= XP_011536934.1:p.Ser764=
XM_011538633.1:c.2150C= XP_011536935.1:p.Ser717=
XM_011538630.2:c.2624C= XP_011536932.2:p.Ser875=
XM_011538631.2:c.2483C= XP_011536933.2:p.Ser828=
XM_011538632.2:c.2444C= XP_011536934.2:p.Ser815=
XM_011538633.2:c.2303C= XP_011536935.2:p.Ser768=
XM_017019774.1:c.2471C= XP_016875263.1:p.Ser824=
NM_021625.5:c.2471C= MANE Select NP_067638.3:p.Ser824=