Canonical Allele Identifier: CA178053

Gene: STRC

Linked Data

• ClinVar Variation Id: 165313
• ClinVar RCV Id: RCV000151952 ; RCV001815209
• dbSNP Id: rs62018890
• ExAC: 15:43900153 C / T
• gnomAD v2: 15-43900153-C-T
• gnomAD v3: 15-43607955-C-T
• gnomAD v4: 15-43607955-C-T
• MyVariant Identifiers: chr15:g.43900153C>T (hg19) ; chr15:g.43607955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43607955C>T , CM000677.2:g.43607955C>T	GRCh38
NC_000015.9:g.43900153C>T , CM000677.1:g.43900153C>T	GRCh37
NC_000015.8:g.41687445C>T	NCBI36
NG_011636.1:g.15846G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.3702G>A MANE Select	ENSP00000401513.2:p.Glu1234=
ENST00000428650.5:c.*734G>A	ENSP00000415991.1:n.*734G>A
ENST00000440125.5:c.*1494G>A	ENSP00000394866.1:n.*1494G>A
ENST00000448437.6:n.1573G>A
ENST00000450892.6:c.3702G>A	ENSP00000401513.2:p.Glu1234=
ENST00000455136.5:c.733G>A
ENST00000471703.5:n.1485G>A
ENST00000485556.5:n.2693G>A
ENST00000541030.5:c.1383G>A	ENSP00000440413.1:p.Glu461=
NM_153700.2:c.3702G>A MANE Select	NP_714544.1:p.Glu1234=
XM_011521277.1:c.4191G>A	XP_011519579.1:p.Glu1397=
XM_011521278.1:c.3807G>A	XP_011519580.1:p.Glu1269=
XM_011521279.1:c.3807G>A	XP_011519581.1:p.Glu1269=