Canonical Allele Identifier: CA16042998

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43610984C>T , CM000677.2:g.43610984C>T	GRCh38
NC_000015.9:g.43903182C>T , CM000677.1:g.43903182C>T	GRCh37
NC_000015.8:g.41690474C>T	NCBI36
NG_011636.1:g.12817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.3307G>A MANE Select	ENSP00000401513.2:p.Val1103Ile
ENST00000428650.5:c.*339G>A	ENSP00000415991.1:n.*339G>A
ENST00000440125.5:c.*1215+515G>A	ENSP00000394866.1:n.*1215+515G>A
ENST00000448437.6:n.697G>A
ENST00000450892.6:c.3307G>A	ENSP00000401513.2:p.Val1103Ile
ENST00000455136.5:c.529+515G>A
ENST00000471703.5:n.609G>A
ENST00000485556.5:n.840G>A
ENST00000541030.5:c.1104+515G>A	ENSP00000440413.1:n.1104+515G>A
NM_153700.2:c.3307G>A MANE Select	NP_714544.1:p.Val1103Ile
XM_011521277.1:c.3796G>A	XP_011519579.1:p.Val1266Ile
XM_011521278.1:c.3409G>A	XP_011519580.1:p.Val1137Ile
XM_011521279.1:c.3409G>A	XP_011519581.1:p.Val1137Ile