Canonical Allele Identifier: CA415786960

Gene: NPHP4

Linked Data

• MyVariant Identifiers: chr1:g.5923974C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.5863914C>G , CM000663.2:g.5863914C>G	GRCh38
NC_000001.10:g.5923974C>G , CM000663.1:g.5923974C>G	GRCh37
NC_000001.9:g.5846561C>G	NCBI36
NG_011724.2:g.133558G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378156.9:c.4116G>C MANE Select	ENSP00000367398.4:p.Leu1372=
ENST00000378156.8:c.4116G>C	ENSP00000367398.4:p.Leu1372=
ENST00000378161.5:n.3267G>C
ENST00000378169.7:c.*3017G>C	ENSP00000367411.3:n.*3017G>C
ENST00000460696.1:n.2864G>C
ENST00000478423.6:n.3848G>C
ENST00000489180.6:c.*1927G>C	ENSP00000423747.1:n.*1927G>C
NM_001291593.1:c.2577G>C	NP_001278522.1:p.Leu859=
NM_001291594.1:c.2580G>C	NP_001278523.1:p.Leu860=
NM_015102.4:c.4116G>C	NP_055917.1:p.Leu1372=
NR_111987.1:n.4931G>C
XM_006710563.2:c.4116G>C	XP_006710626.1:p.Leu1372=
XM_006710565.2:c.4116G>C	XP_006710628.1:p.Leu1372=
XM_011541213.1:c.4113G>C	XP_011539515.1:p.Leu1371=
XM_011541214.1:c.4074G>C	XP_011539516.1:p.Leu1358=
XM_011541215.1:c.4005G>C	XP_011539517.1:p.Leu1335=
XM_011541216.1:c.4116G>C	XP_011539518.1:p.Leu1372=
XM_011541217.1:c.4116G>C	XP_011539519.1:p.Leu1372=
XM_011541218.1:c.4116G>C	XP_011539520.1:p.Leu1372=
XM_011541219.1:c.4062G>C	XP_011539521.1:p.Leu1354=
XM_006710563.3:c.4116G>C	XP_006710626.1:p.Leu1372=
XM_011541216.2:c.4116G>C	XP_011539518.1:p.Leu1372=
XM_011541217.2:c.4116G>C	XP_011539519.1:p.Leu1372=
XM_011541218.2:c.4116G>C	XP_011539520.1:p.Leu1372=
XM_017000996.1:c.4071G>C	XP_016856485.1:p.Leu1357=
XM_017000997.1:c.4116G>C	XP_016856486.1:p.Leu1372=
XM_017000999.1:c.3588G>C	XP_016856488.1:p.Leu1196=
XM_017001000.2:c.3588G>C	XP_016856489.1:p.Leu1196=
XM_017001001.1:c.3318G>C	XP_016856490.1:p.Leu1106=
XM_017001003.1:c.2577G>C	XP_016856492.1:p.Leu859=
XR_001737114.1:n.3982G>C
XR_001737115.1:n.3967G>C
NM_015102.5:c.4116G>C MANE Select	NP_055917.1:p.Leu1372=
NM_001291593.2:c.2577G>C	NP_001278522.1:p.Leu859=
NM_001291594.2:c.2580G>C	NP_001278523.1:p.Leu860=
NR_111987.2:n.4883G>C