Canonical Allele Identifier: CA490148411

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43896571G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604373G>T , CM000677.2:g.43604373G>T	GRCh38
NC_000015.9:g.43896571G>T , CM000677.1:g.43896571G>T	GRCh37
NC_000015.8:g.41683863G>T	NCBI36
NG_011636.1:g.19428C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4206C>A (STRC) MANE Select	ENSP00000401513.2:p.Ser1402=
ENST00000411560.1:n.143-411G>T (CKMT1B)
ENST00000428650.5:c.*1409C>A (STRC)	ENSP00000415991.1:n.*1409C>A
ENST00000440125.5:c.*1998C>A (STRC)	ENSP00000394866.1:n.*1998C>A
ENST00000448437.6:n.1666-2822C>A (STRC)
ENST00000450892.6:c.4206C>A (STRC)	ENSP00000401513.2:p.Ser1402=
ENST00000471703.5:n.2160C>A (STRC)
ENST00000485556.5:n.3061C>A (STRC)
ENST00000541030.5:c.1887C>A (STRC)	ENSP00000440413.1:p.Ser629=
NM_153700.2:c.4206C>A (STRC) MANE Select	NP_714544.1:p.Ser1402=
XM_011521277.1:c.4695C>A (STRC)	XP_011519579.1:p.Ser1565=
XM_011521278.1:c.4311C>A (STRC)	XP_011519580.1:p.Ser1437=
XM_011521279.1:c.4311C>A (STRC)	XP_011519581.1:p.Ser1437=