Canonical Allele Identifier: CA2275179246
Gene: NHERF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763533G= , CM000679.2:g.74763533G= GRCh38
NC_000017.10:g.72759672G= , CM000679.1:g.72759672G= GRCh37
NC_000017.9:g.70271267G= NCBI36
NG_013022.1:g.19910G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262613.10:c.757+13G= MANE Select ENSP00000262613.5:n.757+13G=
ENST00000262613.9:c.757+13G= ENSP00000262613.5:n.757+13G=
ENST00000413388.2:c.289+13G= ENSP00000464982.1:n.289+13G=
ENST00000578958.1:n.491+13G=
ENST00000581356.1:c.93+13G=
ENST00000583369.5:c.442-4614G= ENSP00000464321.1:n.442-4614G=
NM_004252.4:c.757+13G= NP_004243.1:n.757+13G=
XR_002958087.1:n.989G=
NM_004252.5:c.757+13G= MANE Select NP_004243.1:n.757+13G=