Canonical Allele Identifier: CA400939963
Gene: NHERF1 HGNC NCBI

Linked Data

COSMIC: COSM5741121
MyVariant Identifiers: chr17:g.72759504A>G (hg19) chr17:g.74763365A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763365A>G , CM000679.2:g.74763365A>G GRCh38
NC_000017.10:g.72759504A>G , CM000679.1:g.72759504A>G GRCh37
NC_000017.9:g.70271099A>G NCBI36
NG_013022.1:g.19742A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262613.10:c.604-2A>G MANE Select ENSP00000262613.5:n.604-2A>G
ENST00000262613.9:c.604-2A>G ENSP00000262613.5:n.604-2A>G
ENST00000413388.2:c.136-2A>G ENSP00000464982.1:n.136-2A>G
ENST00000578958.1:n.336A>G
ENST00000583369.5:c.442-4782A>G ENSP00000464321.1:n.442-4782A>G
NM_004252.4:c.604-2A>G NP_004243.1:n.604-2A>G
XR_002958087.1:n.823-2A>G
NM_004252.5:c.604-2A>G MANE Select NP_004243.1:n.604-2A>G
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