Canonical Allele Identifier: CA2275179168
Gene: NHERF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763350C= , CM000679.2:g.74763350C= GRCh38
NC_000017.10:g.72759489C= , CM000679.1:g.72759489C= GRCh37
NC_000017.9:g.70271084C= NCBI36
NG_013022.1:g.19727C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262613.10:c.604-17C= MANE Select ENSP00000262613.5:n.604-17C=
ENST00000262613.9:c.604-17C= ENSP00000262613.5:n.604-17C=
ENST00000413388.2:c.136-17C= ENSP00000464982.1:n.136-17C=
ENST00000578958.1:n.321C=
ENST00000583369.5:c.442-4797C= ENSP00000464321.1:n.442-4797C=
NM_004252.4:c.604-17C= NP_004243.1:n.604-17C=
XR_002958087.1:n.823-17C=
NM_004252.5:c.604-17C= MANE Select NP_004243.1:n.604-17C=
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