Canonical Allele Identifier: CA383795574

Gene: NECAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8082376G>C , CM000674.2:g.8082376G>C	GRCh38
NC_000012.11:g.8234972G>C , CM000674.1:g.8234972G>C	GRCh37
NC_000012.10:g.8126239G>C	NCBI36
NG_034155.1:g.5166G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015509.4:c.88G>C MANE Select	NP_056324.2:p.Gly30Arg
ENST00000339754.11:c.88G>C MANE Select	ENSP00000341737.5:p.Gly30Arg
NM_015509.3:c.88G>C	NP_056324.2:p.Gly30Arg
NR_024260.1:n.166G>C
NR_024260.2:n.103G>C
ENST00000339754.9:c.88G>C	ENSP00000341737.5:p.Gly30Arg
ENST00000450991.6:c.88G>C	ENSP00000401963.2:p.Gly30Arg
ENST00000537796.2:n.97G>C
ENST00000541948.1:c.88G>C	ENSP00000440658.1:p.Gly30Arg
ENST00000541948.2:c.88G>C	ENSP00000440658.2:p.Gly30Arg
ENST00000542095.5:n.122G>C
ENST00000542095.6:n.122G>C
ENST00000544891.5:n.107G>C
ENST00000544891.6:n.97G>C
ENST00000545807.5:n.109G>C
ENST00000545807.6:n.69G>C
ENST00000546181.1:n.149G>C
ENST00000546181.2:n.149G>C
ENST00000638237.1:c.88G>C	ENSP00000492254.1:p.Gly30Arg
ENST00000638787.1:c.88G>C	ENSP00000491384.1:p.Gly30Arg
ENST00000638883.1:n.86G>C
ENST00000639038.1:c.88G>C	ENSP00000492452.1:p.Gly30Arg
ENST00000639071.1:n.103G>C
ENST00000639167.1:c.88G>C	ENSP00000490999.1:p.Gly30Arg
ENST00000639276.1:n.109G>C
ENST00000639595.1:c.88G>C	ENSP00000492560.1:p.Gly30Arg
ENST00000639811.1:c.88G>C	ENSP00000492554.1:p.Gly30Arg
ENST00000639955.1:c.88G>C	ENSP00000491067.1:p.Gly30Arg
ENST00000640099.1:n.100G>C
ENST00000640209.1:c.88G>C	ENSP00000492613.1:p.Gly30Arg
ENST00000640481.1:n.77G>C
ENST00000640648.1:n.482G>C