Canonical Allele Identifier: CA2275179250
Gene: NHERF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763541G= , CM000679.2:g.74763541G= GRCh38
NC_000017.10:g.72759680G= , CM000679.1:g.72759680G= GRCh37
NC_000017.9:g.70271275G= NCBI36
NG_013022.1:g.19918G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262613.10:c.757+21G= MANE Select ENSP00000262613.5:n.757+21G=
ENST00000262613.9:c.757+21G= ENSP00000262613.5:n.757+21G=
ENST00000413388.2:c.289+21G= ENSP00000464982.1:n.289+21G=
ENST00000578958.1:n.491+21G=
ENST00000581356.1:c.93+21G=
ENST00000583369.5:c.442-4606G= ENSP00000464321.1:n.442-4606G=
NM_004252.4:c.757+21G= NP_004243.1:n.757+21G=
XR_002958087.1:n.997G=
NM_004252.5:c.757+21G= MANE Select NP_004243.1:n.757+21G=
Search 100 bp 5'
Search 100 bp 3'