Canonical Allele Identifier: CA694750086
Gene: NALF1 HGNC NCBI

Linked Data

dbSNP Id: rs1338993236
gnomAD v3: 13-107427827-C-A
gnomAD v4: 13-107427827-C-A
MyVariant Identifiers: chr13:g.108080175C>A (hg19) chr13:g.107427827C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.107427827C>A , CM000675.2:g.107427827C>A GRCh38
NC_000013.10:g.108080175C>A , CM000675.1:g.108080175C>A GRCh37
NC_000013.9:g.106878176C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375915.4:c.916-217072G>T MANE Select ENSP00000365080.1:n.916-217072G>T
ENST00000375915.3:c.916-217072G>T ENSP00000365080.1:n.916-217072G>T
NM_001080396.2:c.916-217072G>T NP_001073865.1:n.916-217072G>T
XM_011521109.1:c.916-217072G>T XP_011519411.1:n.916-217072G>T
XM_011521109.3:c.916-217072G>T XP_011519411.1:n.916-217072G>T
NM_001080396.3:c.916-217072G>T MANE Select NP_001073865.1:n.916-217072G>T
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