Canonical Allele Identifier: CA2580085775

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109793508_109793514del , CM000674.2:g.109793508_109793514del	GRCh38
NC_000012.11:g.110231313_110231319del , CM000674.1:g.110231313_110231319del	GRCh37
NC_000012.10:g.108715696_108715702del	NCBI36
NG_017090.1:g.44896_44902del , LRG_372:g.44896_44902del

Transcript Alleles

HGVS	Amino-acid Change
NM_021625.5:c.1658+15_1658+21del MANE Select	NP_067638.3:n.1658+15_1658+21del
ENST00000261740.7:c.1658+15_1658+21del MANE Select	ENSP00000261740.2:n.1658+15_1658+21del
NM_001177428.1:c.1517+15_1517+21del	NP_001170899.1:n.1517+15_1517+21del
NM_001177431.1:c.1556+15_1556+21del	NP_001170902.1:n.1556+15_1556+21del
NM_001177433.1:c.1337+15_1337+21del	NP_001170904.1:n.1337+15_1337+21del
NM_021625.4:c.1658+15_1658+21del , LRG_372t1:c.1658+15_1658+21del	NP_067638.3:n.1658+15_1658+21del
NM_147204.2:c.1478+15_1478+21del	NP_671737.1:n.1478+15_1478+21del
ENST00000261740.6:c.1658+15_1658+21del	ENSP00000261740.2:n.1658+15_1658+21del
ENST00000418703.6:c.1658+15_1658+21del	ENSP00000406191.2:n.1658+15_1658+21del
ENST00000418703.7:c.1658+15_1658+21del	ENSP00000406191.2:n.1658+15_1658+21del
ENST00000536838.1:c.1556+15_1556+21del	ENSP00000444336.1:n.1556+15_1556+21del
ENST00000537083.5:c.1478+15_1478+21del	ENSP00000442738.1:n.1478+15_1478+21del
ENST00000538125.5:c.*14_*20del	ENSP00000437449.1:n.*14_*20del
ENST00000541794.5:c.1517+15_1517+21del	ENSP00000442167.1:n.1517+15_1517+21del
ENST00000544971.5:c.1337+15_1337+21del	ENSP00000443611.1:n.1337+15_1337+21del
ENST00000674908.1:c.*745+15_*745+21del	ENSP00000502012.1:n.*745+15_*745+21del
ENST00000675533.1:n.1689+15_1689+21del
ENST00000675670.1:c.1658+15_1658+21del	ENSP00000502135.1:n.1658+15_1658+21del
ENST00000676376.1:n.1689+15_1689+21del
XM_005253918.1:c.1658+15_1658+21del	XP_005253975.1:n.1658+15_1658+21del
XM_011538630.1:c.1658+15_1658+21del	XP_011536932.1:n.1658+15_1658+21del
XM_011538630.2:c.1811+15_1811+21del	XP_011536932.2:n.1811+15_1811+21del
XM_011538631.1:c.1517+15_1517+21del	XP_011536933.1:n.1517+15_1517+21del
XM_011538631.2:c.1670+15_1670+21del	XP_011536933.2:n.1670+15_1670+21del
XM_011538632.1:c.1478+15_1478+21del	XP_011536934.1:n.1478+15_1478+21del
XM_011538632.2:c.1631+15_1631+21del	XP_011536934.2:n.1631+15_1631+21del
XM_011538633.1:c.1337+15_1337+21del	XP_011536935.1:n.1337+15_1337+21del
XM_011538633.2:c.1490+15_1490+21del	XP_011536935.2:n.1490+15_1490+21del
XM_011538634.1:c.1658+15_1658+21del	XP_011536936.1:n.1658+15_1658+21del
XM_011538634.2:c.1811+15_1811+21del	XP_011536936.2:n.1811+15_1811+21del
XM_011538635.1:c.1811+15_1811+21del	XP_011536937.1:n.1811+15_1811+21del
XM_011538635.2:c.1811+15_1811+21del	XP_011536937.1:n.1811+15_1811+21del
XM_011538636.1:c.1811+15_1811+21del	XP_011536938.1:n.1811+15_1811+21del
XM_017019774.1:c.1658+15_1658+21del	XP_016875263.1:n.1658+15_1658+21del