Canonical Allele Identifier: CA338578

Gene: TRPV4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109783739T>C , CM000674.2:g.109783739T>C	GRCh38
NC_000012.11:g.110221544T>C , CM000674.1:g.110221544T>C	GRCh37
NC_000012.10:g.108705927T>C	NCBI36
NG_017090.1:g.54669A>G , LRG_372:g.54669A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261740.7:c.2498A>G MANE Select	ENSP00000261740.2:p.Asn833Ser
ENST00000418703.7:c.2498A>G	ENSP00000406191.2:p.Asn833Ser
ENST00000674908.1:c.*1585A>G	ENSP00000502012.1:n.*1585A>G
ENST00000675670.1:c.2498A>G	ENSP00000502135.1:p.Asn833Ser
ENST00000261740.6:c.2498A>G	ENSP00000261740.2:p.Asn833Ser
ENST00000418703.6:c.2498A>G	ENSP00000406191.2:p.Asn833Ser
ENST00000536838.1:c.2396A>G	ENSP00000444336.1:p.Asn799Ser
ENST00000537083.5:c.2318A>G	ENSP00000442738.1:p.Asn773Ser
ENST00000538125.5:c.*881A>G	ENSP00000437449.1:n.*881A>G
ENST00000541794.5:c.2357A>G	ENSP00000442167.1:p.Asn786Ser
ENST00000544971.5:c.2177A>G	ENSP00000443611.1:p.Asn726Ser
NM_001177428.1:c.2357A>G	NP_001170899.1:p.Asn786Ser
NM_001177431.1:c.2396A>G	NP_001170902.1:p.Asn799Ser
NM_001177433.1:c.2177A>G	NP_001170904.1:p.Asn726Ser
NM_021625.4:c.2498A>G , LRG_372t1:c.2498A>G	NP_067638.3:p.Asn833Ser
NM_147204.2:c.2318A>G	NP_671737.1:p.Asn773Ser
XM_005253918.1:c.2498A>G	XP_005253975.1:p.Asn833Ser
XM_011538630.1:c.2498A>G	XP_011536932.1:p.Asn833Ser
XM_011538631.1:c.2357A>G	XP_011536933.1:p.Asn786Ser
XM_011538632.1:c.2318A>G	XP_011536934.1:p.Asn773Ser
XM_011538633.1:c.2177A>G	XP_011536935.1:p.Asn726Ser
XM_011538630.2:c.2651A>G	XP_011536932.2:p.Asn884Ser
XM_011538631.2:c.2510A>G	XP_011536933.2:p.Asn837Ser
XM_011538632.2:c.2471A>G	XP_011536934.2:p.Asn824Ser
XM_011538633.2:c.2330A>G	XP_011536935.2:p.Asn777Ser
XM_017019774.1:c.2498A>G	XP_016875263.1:p.Asn833Ser
NM_021625.5:c.2498A>G MANE Select	NP_067638.3:p.Asn833Ser