Canonical Allele Identifier: CA481717597

Gene: TRPV4

Linked Data

• MyVariant Identifiers: chr12:g.110234351C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109796546C>A , CM000674.2:g.109796546C>A	GRCh38
NC_000012.11:g.110234351C>A , CM000674.1:g.110234351C>A	GRCh37
NC_000012.10:g.108718734C>A	NCBI36
NG_017090.1:g.41862G>T , LRG_372:g.41862G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261740.7:c.1311G>T MANE Select	ENSP00000261740.2:p.Leu437=
ENST00000418703.7:c.1311G>T	ENSP00000406191.2:p.Leu437=
ENST00000674908.1:c.*398G>T	ENSP00000502012.1:n.*398G>T
ENST00000675533.1:n.1342G>T
ENST00000675670.1:c.1311G>T	ENSP00000502135.1:p.Leu437=
ENST00000676376.1:n.1342G>T
ENST00000261740.6:c.1311G>T	ENSP00000261740.2:p.Leu437=
ENST00000418703.6:c.1311G>T	ENSP00000406191.2:p.Leu437=
ENST00000536838.1:c.1209G>T	ENSP00000444336.1:p.Leu403=
ENST00000537083.5:c.1153-2059G>T	ENSP00000442738.1:n.1153-2059G>T
ENST00000538125.5:c.1311G>T	ENSP00000437449.1:p.Leu437=
ENST00000541794.5:c.1170G>T	ENSP00000442167.1:p.Leu390=
ENST00000544971.5:c.1012-2059G>T	ENSP00000443611.1:n.1012-2059G>T
NM_001177428.1:c.1170G>T	NP_001170899.1:p.Leu390=
NM_001177431.1:c.1209G>T	NP_001170902.1:p.Leu403=
NM_001177433.1:c.1012-2059G>T	NP_001170904.1:n.1012-2059G>T
NM_021625.4:c.1311G>T , LRG_372t1:c.1311G>T	NP_067638.3:p.Leu437=
NM_147204.2:c.1153-2059G>T	NP_671737.1:n.1153-2059G>T
XM_005253918.1:c.1311G>T	XP_005253975.1:p.Leu437=
XM_011538630.1:c.1311G>T	XP_011536932.1:p.Leu437=
XM_011538631.1:c.1170G>T	XP_011536933.1:p.Leu390=
XM_011538632.1:c.1153-2059G>T	XP_011536934.1:n.1153-2059G>T
XM_011538633.1:c.1012-2059G>T	XP_011536935.1:n.1012-2059G>T
XM_011538634.1:c.1311G>T	XP_011536936.1:p.Leu437=
XM_011538635.1:c.1464G>T	XP_011536937.1:p.Leu488=
XM_011538636.1:c.1464G>T	XP_011536938.1:p.Leu488=
XM_011538630.2:c.1464G>T	XP_011536932.2:p.Leu488=
XM_011538631.2:c.1323G>T	XP_011536933.2:p.Leu441=
XM_011538632.2:c.1306-2059G>T	XP_011536934.2:n.1306-2059G>T
XM_011538633.2:c.1165-2059G>T	XP_011536935.2:n.1165-2059G>T
XM_011538634.2:c.1464G>T	XP_011536936.2:p.Leu488=
XM_011538635.2:c.1464G>T	XP_011536937.1:p.Leu488=
XM_017019774.1:c.1311G>T	XP_016875263.1:p.Leu437=
NM_021625.5:c.1311G>T MANE Select	NP_067638.3:p.Leu437=