Canonical Allele Identifier: CA481867571

Gene: TRPV4

Linked Data

• COSMIC: COSM6070974
• MyVariant Identifiers: chr12:g.110236695A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109798890A>G , CM000674.2:g.109798890A>G	GRCh38
NC_000012.11:g.110236695A>G , CM000674.1:g.110236695A>G	GRCh37
NC_000012.10:g.108721078A>G	NCBI36
NG_017090.1:g.39518T>C , LRG_372:g.39518T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.876T>C MANE Select	ENSP00000261740.2:p.Ala292=
ENST00000418703.7:c.876T>C	ENSP00000406191.2:p.Ala292=
ENST00000674908.1:c.905T>C	ENSP00000502012.1:p.Leu302Pro
ENST00000675533.1:n.907T>C
ENST00000675670.1:c.876T>C	ENSP00000502135.1:p.Ala292=
ENST00000676376.1:n.907T>C
ENST00000261740.6:c.876T>C	ENSP00000261740.2:p.Ala292=
ENST00000418703.6:c.876T>C	ENSP00000406191.2:p.Ala292=
ENST00000536838.1:c.774T>C	ENSP00000444336.1:p.Ala258=
ENST00000537083.5:c.876T>C	ENSP00000442738.1:p.Ala292=
ENST00000538125.5:c.876T>C	ENSP00000437449.1:p.Ala292=
ENST00000541794.5:c.735T>C	ENSP00000442167.1:p.Ala245=
ENST00000544971.5:c.735T>C	ENSP00000443611.1:p.Ala245=
NM_001177428.1:c.735T>C	NP_001170899.1:p.Ala245=
NM_001177431.1:c.774T>C	NP_001170902.1:p.Ala258=
NM_001177433.1:c.735T>C	NP_001170904.1:p.Ala245=
NM_021625.4:c.876T>C , LRG_372t1:c.876T>C	NP_067638.3:p.Ala292=
NM_147204.2:c.876T>C	NP_671737.1:p.Ala292=
XM_005253918.1:c.876T>C	XP_005253975.1:p.Ala292=
XM_011538630.1:c.876T>C	XP_011536932.1:p.Ala292=
XM_011538631.1:c.735T>C	XP_011536933.1:p.Ala245=
XM_011538632.1:c.876T>C	XP_011536934.1:p.Ala292=
XM_011538633.1:c.735T>C	XP_011536935.1:p.Ala245=
XM_011538634.1:c.876T>C	XP_011536936.1:p.Ala292=
XM_011538635.1:c.1029T>C	XP_011536937.1:p.Ala343=
XM_011538636.1:c.1029T>C	XP_011536938.1:p.Ala343=
XM_011538630.2:c.1029T>C	XP_011536932.2:p.Ala343=
XM_011538631.2:c.888T>C	XP_011536933.2:p.Ala296=
XM_011538632.2:c.1029T>C	XP_011536934.2:p.Ala343=
XM_011538633.2:c.888T>C	XP_011536935.2:p.Ala296=
XM_011538634.2:c.1029T>C	XP_011536936.2:p.Ala343=
XM_011538635.2:c.1029T>C	XP_011536937.1:p.Ala343=
XM_017019774.1:c.876T>C	XP_016875263.1:p.Ala292=
NM_021625.5:c.876T>C MANE Select	NP_067638.3:p.Ala292=