Canonical Allele Identifier: CA389174492

Gene: HNRNPC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21211813C>T , CM000676.2:g.21211813C>T	GRCh38
NC_000014.8:g.21679972C>T , CM000676.1:g.21679972C>T	GRCh37
NC_000014.7:g.20749812C>T	NCBI36
NG_029011.1:g.62667G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004500.4:c.634G>A MANE Select	NP_004491.2:p.Ala212Thr
ENST00000553300.6:c.634G>A MANE Select	ENSP00000450544.1:p.Ala212Thr
NM_001077442.1:c.673G>A	NP_001070910.1:p.Ala225Thr
NM_001077442.2:c.673G>A	NP_001070910.1:p.Ala225Thr
NM_001077443.1:c.634G>A	NP_001070911.1:p.Ala212Thr
NM_001077443.2:c.634G>A	NP_001070911.1:p.Ala212Thr
NM_004500.3:c.634G>A	NP_004491.2:p.Ala212Thr
NM_031314.2:c.673G>A	NP_112604.2:p.Ala225Thr
NM_031314.3:c.673G>A	NP_112604.2:p.Ala225Thr
ENST00000336053.10:c.634G>A	ENSP00000338095.6:p.Ala212Thr
ENST00000420743.6:c.673G>A	ENSP00000404848.2:p.Ala225Thr
ENST00000430246.6:c.634G>A	ENSP00000442816.1:p.Ala212Thr
ENST00000449098.5:c.634G>A	ENSP00000404559.2:p.Ala212Thr
ENST00000553300.5:c.634G>A	ENSP00000450544.1:p.Ala212Thr
ENST00000553444.1:n.190G>A
ENST00000553753.5:c.634G>A	ENSP00000450548.1:p.Ala212Thr
ENST00000554383.5:c.634G>A	ENSP00000452021.1:p.Ala212Thr
ENST00000554417.1:n.611G>A
ENST00000554455.5:c.673G>A	ENSP00000451291.1:p.Ala225Thr
ENST00000554539.5:c.325G>A	ENSP00000452545.1:p.Ala109Thr
ENST00000554969.5:c.634G>A	ENSP00000450725.1:p.Ala212Thr
ENST00000555309.5:c.673G>A	ENSP00000450790.1:p.Ala225Thr
ENST00000555585.5:n.571G>A
ENST00000555883.5:c.505G>A	ENSP00000450629.1:p.Ala169Thr
ENST00000555914.5:c.634G>A	ENSP00000451708.1:p.Ala212Thr
ENST00000556142.5:c.673G>A	ENSP00000451187.1:p.Ala225Thr
ENST00000556513.5:c.673G>A	ENSP00000452214.1:p.Ala225Thr
ENST00000556628.5:c.433G>A	ENSP00000451652.1:p.Ala145Thr
ENST00000556897.5:c.634G>A	ENSP00000451176.1:p.Ala212Thr
ENST00000557157.5:c.397G>A	ENSP00000450601.1:p.Ala133Thr
ENST00000557201.5:c.673G>A	ENSP00000452276.1:p.Ala225Thr
ENST00000557442.5:c.*108G>A	ENSP00000452599.1:n.*108G>A
XM_006720125.2:c.634G>A	XP_006720188.1:p.Ala212Thr
XM_006720125.3:c.634G>A	XP_006720188.1:p.Ala212Thr
XM_011536708.1:c.673G>A	XP_011535010.1:p.Ala225Thr
XM_011536709.1:c.673G>A	XP_011535011.1:p.Ala225Thr
XM_011536709.3:c.673G>A	XP_011535011.1:p.Ala225Thr
XM_011536710.1:c.673G>A	XP_011535012.1:p.Ala225Thr
XM_011536710.2:c.673G>A	XP_011535012.1:p.Ala225Thr
XM_011536711.1:c.673G>A	XP_011535013.1:p.Ala225Thr
XM_011536711.2:c.673G>A	XP_011535013.1:p.Ala225Thr
XM_011536712.1:c.634G>A	XP_011535014.1:p.Ala212Thr
XM_011536712.2:c.634G>A	XP_011535014.1:p.Ala212Thr
XM_017021252.2:c.634G>A	XP_016876741.1:p.Ala212Thr
XM_017021253.2:c.634G>A	XP_016876742.1:p.Ala212Thr
XM_024449556.1:c.673G>A	XP_024305324.1:p.Ala225Thr
XM_024449557.1:c.673G>A	XP_024305325.1:p.Ala225Thr
XM_024449558.1:c.634G>A	XP_024305326.1:p.Ala212Thr
XM_024449559.1:c.634G>A	XP_024305327.1:p.Ala212Thr