Canonical Allele Identifier: CA386648632

Gene: TRPV4

Linked Data

• MyVariant Identifiers: chr12:g.110221566C>G (hg19) ; chr12:g.109783761C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109783761C>G , CM000674.2:g.109783761C>G	GRCh38
NC_000012.11:g.110221566C>G , CM000674.1:g.110221566C>G	GRCh37
NC_000012.10:g.108705949C>G	NCBI36
NG_017090.1:g.54647G>C , LRG_372:g.54647G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261740.7:c.2476G>C MANE Select	ENSP00000261740.2:p.Val826Leu
ENST00000418703.7:c.2476G>C	ENSP00000406191.2:p.Val826Leu
ENST00000674908.1:c.*1563G>C	ENSP00000502012.1:n.*1563G>C
ENST00000675670.1:c.2476G>C	ENSP00000502135.1:p.Val826Leu
ENST00000261740.6:c.2476G>C	ENSP00000261740.2:p.Val826Leu
ENST00000418703.6:c.2476G>C	ENSP00000406191.2:p.Val826Leu
ENST00000536838.1:c.2374G>C	ENSP00000444336.1:p.Val792Leu
ENST00000537083.5:c.2296G>C	ENSP00000442738.1:p.Val766Leu
ENST00000538125.5:c.*859G>C	ENSP00000437449.1:n.*859G>C
ENST00000541794.5:c.2335G>C	ENSP00000442167.1:p.Val779Leu
ENST00000544971.5:c.2155G>C	ENSP00000443611.1:p.Val719Leu
NM_001177428.1:c.2335G>C	NP_001170899.1:p.Val779Leu
NM_001177431.1:c.2374G>C	NP_001170902.1:p.Val792Leu
NM_001177433.1:c.2155G>C	NP_001170904.1:p.Val719Leu
NM_021625.4:c.2476G>C , LRG_372t1:c.2476G>C	NP_067638.3:p.Val826Leu
NM_147204.2:c.2296G>C	NP_671737.1:p.Val766Leu
XM_005253918.1:c.2476G>C	XP_005253975.1:p.Val826Leu
XM_011538630.1:c.2476G>C	XP_011536932.1:p.Val826Leu
XM_011538631.1:c.2335G>C	XP_011536933.1:p.Val779Leu
XM_011538632.1:c.2296G>C	XP_011536934.1:p.Val766Leu
XM_011538633.1:c.2155G>C	XP_011536935.1:p.Val719Leu
XM_011538630.2:c.2629G>C	XP_011536932.2:p.Val877Leu
XM_011538631.2:c.2488G>C	XP_011536933.2:p.Val830Leu
XM_011538632.2:c.2449G>C	XP_011536934.2:p.Val817Leu
XM_011538633.2:c.2308G>C	XP_011536935.2:p.Val770Leu
XM_017019774.1:c.2476G>C	XP_016875263.1:p.Val826Leu
NM_021625.5:c.2476G>C MANE Select	NP_067638.3:p.Val826Leu