Canonical Allele Identifier: CA2275179208

Gene: NHERF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74763441C= , CM000679.2:g.74763441C=	GRCh38
NC_000017.10:g.72759580C= , CM000679.1:g.72759580C=	GRCh37
NC_000017.9:g.70271175C=	NCBI36
NG_013022.1:g.19818C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262613.10:c.678C= MANE Select	ENSP00000262613.5:p.Thr226=
ENST00000262613.9:c.678C=	ENSP00000262613.5:p.Thr226=
ENST00000413388.2:c.210C=	ENSP00000464982.1:p.Thr70=
ENST00000578958.1:n.412C=
ENST00000581356.1:c.14C=
ENST00000583369.5:c.442-4706C=	ENSP00000464321.1:n.442-4706C=
NM_004252.4:c.678C=	NP_004243.1:p.Thr226=
XR_002958087.1:n.897C=
NM_004252.5:c.678C= MANE Select	NP_004243.1:p.Thr226=