Canonical Allele Identifier: CA270011629

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43610057G>A , CM000677.2:g.43610057G>A	GRCh38
NC_000015.9:g.43902255G>A , CM000677.1:g.43902255G>A	GRCh37
NC_000015.8:g.41689547G>A	NCBI36
NG_011636.1:g.13744C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_153700.2:c.3498+255C>T MANE Select	NP_714544.1:n.3498+255C>T
ENST00000450892.7:c.3498+255C>T MANE Select	ENSP00000401513.2:n.3498+255C>T
ENST00000428650.5:c.*530+255C>T	ENSP00000415991.1:n.*530+255C>T
ENST00000440125.5:c.*1290+255C>T	ENSP00000394866.1:n.*1290+255C>T
ENST00000448437.6:n.1369+255C>T
ENST00000450892.6:c.3498+255C>T	ENSP00000401513.2:n.3498+255C>T
ENST00000455136.5:c.530-723C>T
ENST00000471703.5:n.1281+255C>T
ENST00000485556.5:n.1767C>T
ENST00000541030.5:c.1179+255C>T	ENSP00000440413.1:n.1179+255C>T
XM_011521277.1:c.3987+255C>T	XP_011519579.1:n.3987+255C>T
XM_011521278.1:c.3603+255C>T	XP_011519580.1:n.3603+255C>T
XM_011521279.1:c.3603+255C>T	XP_011519581.1:n.3603+255C>T