Canonical Allele Identifier: CA392157977

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892172C>G (hg19) ; chr15:g.43599974C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599974C>G , CM000677.2:g.43599974C>G	GRCh38
NC_000015.9:g.43892172C>G , CM000677.1:g.43892172C>G	GRCh37
NC_000015.8:g.41679464C>G	NCBI36
NG_011636.1:g.23827G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5225G>C (STRC) MANE Select	ENSP00000401513.2:p.Ser1742Thr
ENST00000411560.1:n.142+441C>G (CKMT1B)
ENST00000428650.5:c.*2258G>C (STRC)	ENSP00000415991.1:n.*2258G>C
ENST00000440125.5:c.*3017G>C (STRC)	ENSP00000394866.1:n.*3017G>C
ENST00000448437.6:n.2345G>C (STRC)
ENST00000450892.6:c.5225G>C (STRC)	ENSP00000401513.2:p.Ser1742Thr
ENST00000471703.5:n.3179G>C (STRC)
ENST00000485556.5:n.4080G>C (STRC)
ENST00000541030.5:c.2906G>C (STRC)	ENSP00000440413.1:p.Ser969Thr
NM_153700.2:c.5225G>C (STRC) MANE Select	NP_714544.1:p.Ser1742Thr
XM_011521277.1:c.5714G>C (STRC)	XP_011519579.1:p.Ser1905Thr
XM_011521278.1:c.5330G>C (STRC)	XP_011519580.1:p.Ser1777Thr
XM_011521279.1:c.5330G>C (STRC)	XP_011519581.1:p.Ser1777Thr