Canonical Allele Identifier: CA671406085
Gene: NPAT HGNC NCBI

Linked Data

dbSNP Id: rs1229632378
MyVariant Identifiers: chr11:g.108090930C>T (hg19) chr11:g.108220203C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108220203C>T , CM000673.2:g.108220203C>T GRCh38
NC_000011.9:g.108090930C>T , CM000673.1:g.108090930C>T GRCh37
NC_000011.8:g.107596140C>T NCBI36
NG_009830.1:g.2372C>T , LRG_135:g.2372C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278612.9:c.37+2297G>A MANE Select ENSP00000278612.8:n.37+2297G>A
ENST00000278612.8:c.37+2297G>A ENSP00000278612.8:n.37+2297G>A
ENST00000531384.1:c.37+2297G>A ENSP00000433497.1:n.37+2297G>A
ENST00000610253.5:n.137+2297G>A
NM_002519.2:c.37+2297G>A NP_002510.2:n.37+2297G>A
XM_011542854.1:c.37+2297G>A XP_011541156.1:n.37+2297G>A
XM_011542855.1:c.37+2297G>A XP_011541157.1:n.37+2297G>A
NM_001321307.1:c.37+2297G>A NP_001308236.1:n.37+2297G>A
XM_011542854.2:c.37+2297G>A XP_011541156.1:n.37+2297G>A
NM_002519.3:c.37+2297G>A MANE Select NP_002510.2:n.37+2297G>A
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