Canonical Allele Identifier: CA392163562

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43601430-G-T
• MyVariant Identifiers: chr15:g.43893628G>T (hg19) ; chr15:g.43601430G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601430G>T , CM000677.2:g.43601430G>T	GRCh38
NC_000015.9:g.43893628G>T , CM000677.1:g.43893628G>T	GRCh37
NC_000015.8:g.41680920G>T	NCBI36
NG_011636.1:g.22371C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4667C>A (STRC) MANE Select	ENSP00000401513.2:p.Thr1556Asn
ENST00000411560.1:n.142+1897G>T (CKMT1B)
ENST00000428650.5:c.*1700C>A (STRC)	ENSP00000415991.1:n.*1700C>A
ENST00000440125.5:c.*2459C>A (STRC)	ENSP00000394866.1:n.*2459C>A
ENST00000448437.6:n.1787C>A (STRC)
ENST00000450892.6:c.4667C>A (STRC)	ENSP00000401513.2:p.Thr1556Asn
ENST00000460952.1:n.246C>A (STRC)
ENST00000471703.5:n.2621C>A (STRC)
ENST00000485556.5:n.3522C>A (STRC)
ENST00000493750.1:n.463C>A (STRC)
ENST00000541030.5:c.2348C>A (STRC)	ENSP00000440413.1:p.Thr783Asn
NM_153700.2:c.4667C>A (STRC) MANE Select	NP_714544.1:p.Thr1556Asn
XM_011521277.1:c.5156C>A (STRC)	XP_011519579.1:p.Thr1719Asn
XM_011521278.1:c.4772C>A (STRC)	XP_011519580.1:p.Thr1591Asn
XM_011521279.1:c.4772C>A (STRC)	XP_011519581.1:p.Thr1591Asn