Canonical Allele Identifier: CA694750081
Gene: NALF1 HGNC NCBI

Linked Data

dbSNP Id: rs1251222298
MyVariant Identifiers: chr13:g.108080152T>G (hg19) chr13:g.107427804T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.107427804T>G , CM000675.2:g.107427804T>G GRCh38
NC_000013.10:g.108080152T>G , CM000675.1:g.108080152T>G GRCh37
NC_000013.9:g.106878153T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375915.4:c.916-217049A>C MANE Select ENSP00000365080.1:n.916-217049A>C
ENST00000375915.3:c.916-217049A>C ENSP00000365080.1:n.916-217049A>C
NM_001080396.2:c.916-217049A>C NP_001073865.1:n.916-217049A>C
XM_011521109.1:c.916-217049A>C XP_011519411.1:n.916-217049A>C
XM_011521109.3:c.916-217049A>C XP_011519411.1:n.916-217049A>C
NM_001080396.3:c.916-217049A>C MANE Select NP_001073865.1:n.916-217049A>C
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