Canonical Allele Identifier: CA343566497

Gene: NPHS2 AXDND1

Linked Data

• MyVariant Identifiers: chr1:g.179523651C>T (hg19) ; chr1:g.179554516C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179554516C>T , CM000663.2:g.179554516C>T	GRCh38
NC_000001.10:g.179523651C>T , CM000663.1:g.179523651C>T	GRCh37
NC_000001.9:g.177790274C>T	NCBI36
NG_007535.1:g.26434G>A , LRG_887:g.26434G>A
NG_033075.1:g.193797C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.754G>A (NPHS2) MANE Select	ENSP00000356587.4:p.Val252Met
ENST00000367618.8:c.3036C>T (AXDND1) MANE Select	ENSP00000356590.3:p.His1012=
ENST00000367615.8:c.754G>A (NPHS2)	ENSP00000356587.4:p.Val252Met
ENST00000367616.4:c.550G>A (NPHS2)	ENSP00000356588.4:p.Val184Met
ENST00000367618.7:c.3036C>T (AXDND1)	ENSP00000356590.3:p.His1012=
ENST00000434088.1:c.2616C>T (AXDND1)	ENSP00000391716.1:p.His872=
ENST00000457238.6:c.*1015C>T (AXDND1)	ENSP00000416712.3:n.*1015C>T
ENST00000484455.1:n.475C>T (AXDND1)
ENST00000484883.1:n.915C>T (AXDND1)
ENST00000489080.1:n.1640C>T (AXDND1)
ENST00000511157.5:c.*1305C>T (AXDND1)	ENSP00000424373.1:n.*1305C>T
ENST00000617277.4:c.*1211C>T (AXDND1)	ENSP00000482167.1:n.*1211C>T
NM_001297575.1:c.550G>A (NPHS2)	NP_001284504.1:p.Val184Met
NM_014625.3:c.754G>A , LRG_887t1:c.754G>A (NPHS2)	NP_055440.1:p.Val252Met
NM_144696.5:c.3036C>T (AXDND1)	NP_653297.3:p.His1012=
NR_073544.1:n.3156C>T (AXDND1)
XM_005245483.2:c.577G>A (NPHS2)	XP_005245540.1:p.Val193Met
XM_006711529.2:c.754G>A (NPHS2)	XP_006711592.1:p.Val252Met
XM_011509165.1:c.3042C>T (AXDND1)	XP_011507467.1:p.His1014=
XM_011509166.1:c.3042C>T (AXDND1)	XP_011507468.1:p.His1014=
XM_011509167.1:c.3042C>T (AXDND1)	XP_011507469.1:p.His1014=
XM_011509168.1:c.3042C>T (AXDND1)	XP_011507470.1:p.His1014=
XM_011509169.1:c.2979C>T (AXDND1)	XP_011507471.1:p.His993=
XM_011509170.1:c.2934C>T (AXDND1)	XP_011507472.1:p.His978=
XM_011509171.1:c.2916C>T (AXDND1)	XP_011507473.1:p.His972=
XM_011509172.1:c.2916C>T (AXDND1)	XP_011507474.1:p.His972=
XM_011509173.1:c.2916C>T (AXDND1)	XP_011507475.1:p.His972=
XM_011509174.1:c.2820C>T (AXDND1)	XP_011507476.1:p.His940=
XM_011509175.1:c.2814C>T (AXDND1)	XP_011507477.1:p.His938=
XM_011509176.1:c.2745C>T (AXDND1)	XP_011507478.1:p.His915=
XM_011509179.1:c.2406C>T (AXDND1)	XP_011507481.1:p.His802=
XM_011509181.1:c.1965C>T (AXDND1)	XP_011507483.1:p.His655=
XM_005245483.3:c.577G>A (NPHS2)	XP_005245540.1:p.Val193Met
XM_011509166.3:c.3042C>T (AXDND1)	XP_011507468.1:p.His1014=
XM_011509167.3:c.3042C>T (AXDND1)	XP_011507469.1:p.His1014=
XM_011509179.2:c.2406C>T (AXDND1)	XP_011507481.1:p.His802=
XM_011509181.2:c.1965C>T (AXDND1)	XP_011507483.1:p.His655=
XM_017000257.2:c.2301C>T (AXDND1)	XP_016855746.1:p.His767=
XM_017000258.2:c.2163C>T (AXDND1)	XP_016855747.1:p.His721=
XM_017002298.1:c.462-1835G>A (NPHS2)	XP_016857787.1:n.462-1835G>A
XM_017002299.1:c.535-1835G>A (NPHS2)	XP_016857788.1:n.535-1835G>A
XM_024453104.1:c.2916C>T (AXDND1)	XP_024308872.1:p.His972=
XM_024453107.1:c.2916C>T (AXDND1)	XP_024308875.1:p.His972=
NM_144696.6:c.3036C>T (AXDND1) MANE Select	NP_653297.3:p.His1012=
NM_001297575.2:c.550G>A (NPHS2)	NP_001284504.1:p.Val184Met
NM_014625.4:c.754G>A (NPHS2) MANE Select	NP_055440.1:p.Val252Met
NR_073544.2:n.3084C>T (AXDND1)