Canonical Allele Identifier: CA400939971
Gene: NHERF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.72759507T>G (hg19) chr17:g.74763368T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763368T>G , CM000679.2:g.74763368T>G GRCh38
NC_000017.10:g.72759507T>G , CM000679.1:g.72759507T>G GRCh37
NC_000017.9:g.70271102T>G NCBI36
NG_013022.1:g.19745T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262613.10:c.605T>G MANE Select ENSP00000262613.5:p.Val202Gly
ENST00000262613.9:c.605T>G ENSP00000262613.5:p.Val202Gly
ENST00000413388.2:c.137T>G ENSP00000464982.1:p.Val46Gly
ENST00000578958.1:n.339T>G
ENST00000583369.5:c.442-4779T>G ENSP00000464321.1:n.442-4779T>G
NM_004252.4:c.605T>G NP_004243.1:p.Val202Gly
XR_002958087.1:n.824T>G
NM_004252.5:c.605T>G MANE Select NP_004243.1:p.Val202Gly
Search 100 bp 5'
Search 100 bp 3'