Canonical Allele Identifier: CA400940488

Gene: NHERF1

Linked Data

• MyVariant Identifiers: chr17:g.72759656A>T (hg19) ; chr17:g.74763517A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74763517A>T , CM000679.2:g.74763517A>T	GRCh38
NC_000017.10:g.72759656A>T , CM000679.1:g.72759656A>T	GRCh37
NC_000017.9:g.70271251A>T	NCBI36
NG_013022.1:g.19894A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262613.10:c.754A>T MANE Select	ENSP00000262613.5:p.Asn252Tyr
ENST00000262613.9:c.754A>T	ENSP00000262613.5:p.Asn252Tyr
ENST00000413388.2:c.286A>T	ENSP00000464982.1:p.Asn96Tyr
ENST00000578958.1:n.488A>T
ENST00000581356.1:c.90A>T
ENST00000583369.5:c.442-4630A>T	ENSP00000464321.1:n.442-4630A>T
NM_004252.4:c.754A>T	NP_004243.1:p.Asn252Tyr
XR_002958087.1:n.973A>T
NM_004252.5:c.754A>T MANE Select	NP_004243.1:p.Asn252Tyr