Canonical Allele Identifier: CA386648921

Gene: TRPV4

Linked Data

• MyVariant Identifiers: chr12:g.110222228T>A (hg19) ; chr12:g.109784423T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109784423T>A , CM000674.2:g.109784423T>A	GRCh38
NC_000012.11:g.110222228T>A , CM000674.1:g.110222228T>A	GRCh37
NC_000012.10:g.108706611T>A	NCBI36
NG_017090.1:g.53985A>T , LRG_372:g.53985A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.2351A>T MANE Select	ENSP00000261740.2:p.Asn784Ile
ENST00000418703.7:c.2351A>T	ENSP00000406191.2:p.Asn784Ile
ENST00000674908.1:c.*1438A>T	ENSP00000502012.1:n.*1438A>T
ENST00000675670.1:c.2351A>T	ENSP00000502135.1:p.Asn784Ile
ENST00000261740.6:c.2351A>T	ENSP00000261740.2:p.Asn784Ile
ENST00000418703.6:c.2351A>T	ENSP00000406191.2:p.Asn784Ile
ENST00000536838.1:c.2249A>T	ENSP00000444336.1:p.Asn750Ile
ENST00000537083.5:c.2171A>T	ENSP00000442738.1:p.Asn724Ile
ENST00000538125.5:c.*734A>T	ENSP00000437449.1:n.*734A>T
ENST00000541794.5:c.2210A>T	ENSP00000442167.1:p.Asn737Ile
ENST00000544971.5:c.2030A>T	ENSP00000443611.1:p.Asn677Ile
NM_001177428.1:c.2210A>T	NP_001170899.1:p.Asn737Ile
NM_001177431.1:c.2249A>T	NP_001170902.1:p.Asn750Ile
NM_001177433.1:c.2030A>T	NP_001170904.1:p.Asn677Ile
NM_021625.4:c.2351A>T , LRG_372t1:c.2351A>T	NP_067638.3:p.Asn784Ile
NM_147204.2:c.2171A>T	NP_671737.1:p.Asn724Ile
XM_005253918.1:c.2351A>T	XP_005253975.1:p.Asn784Ile
XM_011538630.1:c.2351A>T	XP_011536932.1:p.Asn784Ile
XM_011538631.1:c.2210A>T	XP_011536933.1:p.Asn737Ile
XM_011538632.1:c.2171A>T	XP_011536934.1:p.Asn724Ile
XM_011538633.1:c.2030A>T	XP_011536935.1:p.Asn677Ile
XM_011538630.2:c.2504A>T	XP_011536932.2:p.Asn835Ile
XM_011538631.2:c.2363A>T	XP_011536933.2:p.Asn788Ile
XM_011538632.2:c.2324A>T	XP_011536934.2:p.Asn775Ile
XM_011538633.2:c.2183A>T	XP_011536935.2:p.Asn728Ile
XM_017019774.1:c.2351A>T	XP_016875263.1:p.Asn784Ile
NM_021625.5:c.2351A>T MANE Select	NP_067638.3:p.Asn784Ile