Canonical Allele Identifier: CA2117616998
Gene: NALF1 HGNC NCBI
NALF1-IT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.107832106G= , CM000675.2:g.107832106G= GRCh38
NC_000013.10:g.108484454G= , CM000675.1:g.108484454G= GRCh37
NC_000013.9:g.107282455G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375915.4:c.915+33576C= (NALF1) MANE Select ENSP00000365080.1:n.915+33576C=
ENST00000375915.3:c.915+33576C= (NALF1) ENSP00000365080.1:n.915+33576C=
NM_001080396.2:c.915+33576C= (NALF1) NP_001073865.1:n.915+33576C=
NR_046848.1:n.57+3296C= (NALF1-IT1)
XM_011521109.1:c.915+33576C= (NALF1) XP_011519411.1:n.915+33576C=
XM_011521109.3:c.915+33576C= (NALF1) XP_011519411.1:n.915+33576C=
NM_001080396.3:c.915+33576C= (NALF1) MANE Select NP_001073865.1:n.915+33576C=