Canonical Allele Identifier: CA2275179169
Gene: NHERF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763351C= , CM000679.2:g.74763351C= GRCh38
NC_000017.10:g.72759490C= , CM000679.1:g.72759490C= GRCh37
NC_000017.9:g.70271085C= NCBI36
NG_013022.1:g.19728C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262613.10:c.604-16C= MANE Select ENSP00000262613.5:n.604-16C=
ENST00000262613.9:c.604-16C= ENSP00000262613.5:n.604-16C=
ENST00000413388.2:c.136-16C= ENSP00000464982.1:n.136-16C=
ENST00000578958.1:n.322C=
ENST00000583369.5:c.442-4796C= ENSP00000464321.1:n.442-4796C=
NM_004252.4:c.604-16C= NP_004243.1:n.604-16C=
XR_002958087.1:n.823-16C=
NM_004252.5:c.604-16C= MANE Select NP_004243.1:n.604-16C=