Canonical Allele Identifier: CA507091304

Gene: NPHS1

Linked Data

• MyVariant Identifiers: chr19:g.36317461C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35826559C>G , CM000681.2:g.35826559C>G	GRCh38
NC_000019.9:g.36317461C>G , CM000681.1:g.36317461C>G	GRCh37
NC_000019.8:g.41009301C>G	NCBI36
NG_013356.2:g.47729G>C , LRG_693:g.47729G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378910.10:c.3681G>C MANE Select	ENSP00000368190.4:p.Leu1227=
ENST00000353632.6:c.3561G>C	ENSP00000343634.5:p.Leu1187=
ENST00000378910.9:c.3681G>C	ENSP00000368190.4:p.Leu1227=
NM_004646.3:c.3681G>C , LRG_693t1:c.3681G>C	NP_004637.1:p.Leu1227=
NM_004646.4:c.3681G>C MANE Select	NP_004637.1:p.Leu1227=