Canonical Allele Identifier: CA386651802

Gene: TRPV4

Linked Data

• MyVariant Identifiers: chr12:g.110230210A>C (hg19) ; chr12:g.109792405A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109792405A>C , CM000674.2:g.109792405A>C	GRCh38
NC_000012.11:g.110230210A>C , CM000674.1:g.110230210A>C	GRCh37
NC_000012.10:g.108714593A>C	NCBI36
NG_017090.1:g.46003T>G , LRG_372:g.46003T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.1849T>G MANE Select	ENSP00000261740.2:p.Phe617Val
ENST00000418703.7:c.1849T>G	ENSP00000406191.2:p.Phe617Val
ENST00000674908.1:c.*936T>G	ENSP00000502012.1:n.*936T>G
ENST00000675533.1:n.1880T>G
ENST00000675670.1:c.1849T>G	ENSP00000502135.1:p.Phe617Val
ENST00000676376.1:n.1880T>G
ENST00000261740.6:c.1849T>G	ENSP00000261740.2:p.Phe617Val
ENST00000418703.6:c.1849T>G	ENSP00000406191.2:p.Phe617Val
ENST00000536838.1:c.1747T>G	ENSP00000444336.1:p.Phe583Val
ENST00000537083.5:c.1669T>G	ENSP00000442738.1:p.Phe557Val
ENST00000538125.5:c.*232T>G	ENSP00000437449.1:n.*232T>G
ENST00000541794.5:c.1708T>G	ENSP00000442167.1:p.Phe570Val
ENST00000544971.5:c.1528T>G	ENSP00000443611.1:p.Phe510Val
NM_001177428.1:c.1708T>G	NP_001170899.1:p.Phe570Val
NM_001177431.1:c.1747T>G	NP_001170902.1:p.Phe583Val
NM_001177433.1:c.1528T>G	NP_001170904.1:p.Phe510Val
NM_021625.4:c.1849T>G , LRG_372t1:c.1849T>G	NP_067638.3:p.Phe617Val
NM_147204.2:c.1669T>G	NP_671737.1:p.Phe557Val
XM_005253918.1:c.1849T>G	XP_005253975.1:p.Phe617Val
XM_011538630.1:c.1849T>G	XP_011536932.1:p.Phe617Val
XM_011538631.1:c.1708T>G	XP_011536933.1:p.Phe570Val
XM_011538632.1:c.1669T>G	XP_011536934.1:p.Phe557Val
XM_011538633.1:c.1528T>G	XP_011536935.1:p.Phe510Val
XM_011538634.1:c.1849T>G	XP_011536936.1:p.Phe617Val
XM_011538635.1:c.2002T>G	XP_011536937.1:p.Phe668Val
XM_011538630.2:c.2002T>G	XP_011536932.2:p.Phe668Val
XM_011538631.2:c.1861T>G	XP_011536933.2:p.Phe621Val
XM_011538632.2:c.1822T>G	XP_011536934.2:p.Phe608Val
XM_011538633.2:c.1681T>G	XP_011536935.2:p.Phe561Val
XM_011538634.2:c.2002T>G	XP_011536936.2:p.Phe668Val
XM_011538635.2:c.2002T>G	XP_011536937.1:p.Phe668Val
XM_017019774.1:c.1849T>G	XP_016875263.1:p.Phe617Val
NM_021625.5:c.1849T>G MANE Select	NP_067638.3:p.Phe617Val