Canonical Allele Identifier: CA2275179162
Gene: NHERF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763338C= , CM000679.2:g.74763338C= GRCh38
NC_000017.10:g.72759477C= , CM000679.1:g.72759477C= GRCh37
NC_000017.9:g.70271072C= NCBI36
NG_013022.1:g.19715C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262613.10:c.604-29C= MANE Select ENSP00000262613.5:n.604-29C=
ENST00000262613.9:c.604-29C= ENSP00000262613.5:n.604-29C=
ENST00000413388.2:c.136-29C= ENSP00000464982.1:n.136-29C=
ENST00000578958.1:n.309C=
ENST00000583369.5:c.442-4809C= ENSP00000464321.1:n.442-4809C=
NM_004252.4:c.604-29C= NP_004243.1:n.604-29C=
XR_002958087.1:n.823-29C=
NM_004252.5:c.604-29C= MANE Select NP_004243.1:n.604-29C=
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