Canonical Allele Identifier: CA7528338

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43610350G>A , CM000677.2:g.43610350G>A	GRCh38
NC_000015.9:g.43902548G>A , CM000677.1:g.43902548G>A	GRCh37
NC_000015.8:g.41689840G>A	NCBI36
NG_011636.1:g.13451C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.3460C>T MANE Select	ENSP00000401513.2:p.Arg1154Ter
ENST00000428650.5:c.*492C>T	ENSP00000415991.1:n.*492C>T
ENST00000440125.5:c.*1252C>T	ENSP00000394866.1:n.*1252C>T
ENST00000448437.6:n.1331C>T
ENST00000450892.6:c.3460C>T	ENSP00000401513.2:p.Arg1154Ter
ENST00000455136.5:c.530-1016C>T
ENST00000471703.5:n.1243C>T
ENST00000485556.5:n.1474C>T
ENST00000541030.5:c.1141C>T	ENSP00000440413.1:p.Arg381Ter
NM_153700.2:c.3460C>T MANE Select	NP_714544.1:p.Arg1154Ter
XM_011521277.1:c.3949C>T	XP_011519579.1:p.Arg1317Ter
XM_011521278.1:c.3565C>T	XP_011519580.1:p.Arg1189Ter
XM_011521279.1:c.3565C>T	XP_011519581.1:p.Arg1189Ter