Canonical Allele Identifier: CA210886
Gene: NECAP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8089982C>T , CM000674.2:g.8089982C>T GRCh38
NC_000012.11:g.8242578C>T , CM000674.1:g.8242578C>T GRCh37
NC_000012.10:g.8133845C>T NCBI36
NG_034155.1:g.12772C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339754.11:c.142C>T MANE Select ENSP00000341737.5:p.Arg48Ter
ENST00000537796.2:n.151C>T
ENST00000541948.2:c.142C>T ENSP00000440658.2:p.Arg48Ter
ENST00000542095.6:n.176C>T
ENST00000544891.6:n.151C>T
ENST00000545807.6:n.123C>T
ENST00000546181.2:n.203C>T
ENST00000638237.1:c.142C>T ENSP00000492254.1:p.Arg48Ter
ENST00000638787.1:c.142C>T ENSP00000491384.1:p.Arg48Ter
ENST00000638883.1:n.140C>T
ENST00000639038.1:c.142C>T ENSP00000492452.1:p.Arg48Ter
ENST00000639071.1:n.157C>T
ENST00000639167.1:c.96-2694C>T ENSP00000490999.1:n.96-2694C>T
ENST00000639276.1:n.163C>T
ENST00000639595.1:c.142C>T ENSP00000492560.1:p.Arg48Ter
ENST00000639811.1:c.142C>T ENSP00000492554.1:p.Arg48Ter
ENST00000639955.1:c.142C>T ENSP00000491067.1:p.Arg48Ter
ENST00000640072.1:n.1093C>T
ENST00000640099.1:n.154C>T
ENST00000640209.1:c.142C>T ENSP00000492613.1:p.Arg48Ter
ENST00000640481.1:n.131C>T
ENST00000640648.1:n.536C>T
ENST00000339754.9:c.142C>T ENSP00000341737.5:p.Arg48Ter
ENST00000450991.6:c.142C>T ENSP00000401963.2:p.Arg48Ter
ENST00000540083.1:c.-285C>T ENSP00000439319.1:n.-285C>T
ENST00000541948.1:c.142C>T ENSP00000440658.1:p.Arg48Ter
ENST00000542095.5:n.176C>T
ENST00000544891.5:n.161C>T
ENST00000545807.5:n.163C>T
ENST00000546181.1:n.203C>T
NM_015509.3:c.142C>T NP_056324.2:p.Arg48Ter
NR_024260.1:n.220C>T
NM_015509.4:c.142C>T MANE Select NP_056324.2:p.Arg48Ter
NR_024260.2:n.157C>T
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