Canonical Allele Identifier: CA386651799

Gene: TRPV4

Linked Data

• MyVariant Identifiers: chr12:g.110230209A>C (hg19) ; chr12:g.109792404A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109792404A>C , CM000674.2:g.109792404A>C	GRCh38
NC_000012.11:g.110230209A>C , CM000674.1:g.110230209A>C	GRCh37
NC_000012.10:g.108714592A>C	NCBI36
NG_017090.1:g.46004T>G , LRG_372:g.46004T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261740.7:c.1850T>G MANE Select	ENSP00000261740.2:p.Phe617Cys
ENST00000418703.7:c.1850T>G	ENSP00000406191.2:p.Phe617Cys
ENST00000674908.1:c.*937T>G	ENSP00000502012.1:n.*937T>G
ENST00000675533.1:n.1881T>G
ENST00000675670.1:c.1850T>G	ENSP00000502135.1:p.Phe617Cys
ENST00000676376.1:n.1881T>G
ENST00000261740.6:c.1850T>G	ENSP00000261740.2:p.Phe617Cys
ENST00000418703.6:c.1850T>G	ENSP00000406191.2:p.Phe617Cys
ENST00000536838.1:c.1748T>G	ENSP00000444336.1:p.Phe583Cys
ENST00000537083.5:c.1670T>G	ENSP00000442738.1:p.Phe557Cys
ENST00000538125.5:c.*233T>G	ENSP00000437449.1:n.*233T>G
ENST00000541794.5:c.1709T>G	ENSP00000442167.1:p.Phe570Cys
ENST00000544971.5:c.1529T>G	ENSP00000443611.1:p.Phe510Cys
NM_001177428.1:c.1709T>G	NP_001170899.1:p.Phe570Cys
NM_001177431.1:c.1748T>G	NP_001170902.1:p.Phe583Cys
NM_001177433.1:c.1529T>G	NP_001170904.1:p.Phe510Cys
NM_021625.4:c.1850T>G , LRG_372t1:c.1850T>G	NP_067638.3:p.Phe617Cys
NM_147204.2:c.1670T>G	NP_671737.1:p.Phe557Cys
XM_005253918.1:c.1850T>G	XP_005253975.1:p.Phe617Cys
XM_011538630.1:c.1850T>G	XP_011536932.1:p.Phe617Cys
XM_011538631.1:c.1709T>G	XP_011536933.1:p.Phe570Cys
XM_011538632.1:c.1670T>G	XP_011536934.1:p.Phe557Cys
XM_011538633.1:c.1529T>G	XP_011536935.1:p.Phe510Cys
XM_011538634.1:c.1850T>G	XP_011536936.1:p.Phe617Cys
XM_011538635.1:c.2003T>G	XP_011536937.1:p.Phe668Cys
XM_011538630.2:c.2003T>G	XP_011536932.2:p.Phe668Cys
XM_011538631.2:c.1862T>G	XP_011536933.2:p.Phe621Cys
XM_011538632.2:c.1823T>G	XP_011536934.2:p.Phe608Cys
XM_011538633.2:c.1682T>G	XP_011536935.2:p.Phe561Cys
XM_011538634.2:c.2003T>G	XP_011536936.2:p.Phe668Cys
XM_011538635.2:c.2003T>G	XP_011536937.1:p.Phe668Cys
XM_017019774.1:c.1850T>G	XP_016875263.1:p.Phe617Cys
NM_021625.5:c.1850T>G MANE Select	NP_067638.3:p.Phe617Cys