Canonical Allele Identifier: CA5694612

Gene: NRAP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113605772A>G , CM000672.2:g.113605772A>G	GRCh38
NC_000010.10:g.115365531A>G , CM000672.1:g.115365531A>G	GRCh37
NC_000010.9:g.115355521A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_198060.4:c.3905T>C MANE Select	NP_932326.2:p.Ile1302Thr
ENST00000359988.4:c.3905T>C MANE Select	ENSP00000353078.3:p.Ile1302Thr
NM_001261463.1:c.3905T>C	NP_001248392.1:p.Ile1302Thr
NM_001261463.2:c.3905T>C	NP_001248392.1:p.Ile1302Thr
NM_001322945.1:c.3797T>C	NP_001309874.1:p.Ile1266Thr
NM_001322945.2:c.3797T>C	NP_001309874.1:p.Ile1266Thr
NM_006175.4:c.3800T>C	NP_006166.3:p.Ile1267Thr
NM_006175.5:c.3800T>C	NP_006166.3:p.Ile1267Thr
NM_198060.3:c.3905T>C	NP_932326.2:p.Ile1302Thr
ENST00000359988.3:c.3905T>C	ENSP00000353078.2:p.Ile1302Thr
ENST00000360478.7:c.3800T>C	ENSP00000353666.3:p.Ile1267Thr
ENST00000369358.8:c.3905T>C	ENSP00000358365.4:p.Ile1302Thr
ENST00000369360.7:c.3824T>C	ENSP00000358367.3:p.Ile1275Thr
XM_005269864.1:c.3800T>C	XP_005269921.1:p.Ile1267Thr
XM_005269864.2:c.3800T>C	XP_005269921.1:p.Ile1267Thr
XM_005269865.1:c.3797T>C	XP_005269922.1:p.Ile1266Thr
XM_005269865.2:c.3797T>C	XP_005269922.1:p.Ile1266Thr
XM_005269867.1:c.3905T>C	XP_005269924.1:p.Ile1302Thr
XM_005269867.2:c.3905T>C	XP_005269924.1:p.Ile1302Thr
XM_006717870.1:c.3800T>C	XP_006717933.1:p.Ile1267Thr
XM_006717870.2:c.3800T>C	XP_006717933.1:p.Ile1267Thr
XM_011539832.1:c.3905T>C	XP_011538134.1:p.Ile1302Thr
XM_011539832.2:c.3905T>C	XP_011538134.1:p.Ile1302Thr
XM_024448029.1:c.3905T>C	XP_024303797.1:p.Ile1302Thr