Canonical Allele Identifier: CA2275179211
Gene: NHERF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763448C= , CM000679.2:g.74763448C= GRCh38
NC_000017.10:g.72759587C= , CM000679.1:g.72759587C= GRCh37
NC_000017.9:g.70271182C= NCBI36
NG_013022.1:g.19825C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262613.10:c.685C= MANE Select ENSP00000262613.5:p.Leu229=
ENST00000262613.9:c.685C= ENSP00000262613.5:p.Leu229=
ENST00000413388.2:c.217C= ENSP00000464982.1:p.Leu73=
ENST00000578958.1:n.419C=
ENST00000581356.1:c.21C=
ENST00000583369.5:c.442-4699C= ENSP00000464321.1:n.442-4699C=
NM_004252.4:c.685C= NP_004243.1:p.Leu229=
XR_002958087.1:n.904C=
NM_004252.5:c.685C= MANE Select NP_004243.1:p.Leu229=