Canonical Allele Identifier: CA2333842014
Gene: NPHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35831122A= , CM000681.2:g.35831122A= GRCh38
NC_000019.9:g.36322024A= , CM000681.1:g.36322024A= GRCh37
NC_000019.8:g.41013864A= NCBI36
NG_013356.2:g.43166T= , LRG_693:g.43166T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.3412T= MANE Select ENSP00000368190.4:p.Tyr1138=
ENST00000353632.6:c.3292T= ENSP00000343634.5:p.Tyr1098=
ENST00000378910.9:c.3412T= ENSP00000368190.4:p.Tyr1138=
NM_004646.3:c.3412T= , LRG_693t1:c.3412T= NP_004637.1:p.Tyr1138=
NM_004646.4:c.3412T= MANE Select NP_004637.1:p.Tyr1138=