Canonical Allele Identifier: CA392162579

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893082C>G (hg19) ; chr15:g.43600884C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600884C>G , CM000677.2:g.43600884C>G	GRCh38
NC_000015.9:g.43893082C>G , CM000677.1:g.43893082C>G	GRCh37
NC_000015.8:g.41680374C>G	NCBI36
NG_011636.1:g.22917G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4832G>C (STRC) MANE Select	ENSP00000401513.2:p.Ser1611Thr
ENST00000411560.1:n.142+1351C>G (CKMT1B)
ENST00000428650.5:c.*1865G>C (STRC)	ENSP00000415991.1:n.*1865G>C
ENST00000440125.5:c.*2624G>C (STRC)	ENSP00000394866.1:n.*2624G>C
ENST00000448437.6:n.1952G>C (STRC)
ENST00000450892.6:c.4832G>C (STRC)	ENSP00000401513.2:p.Ser1611Thr
ENST00000460952.1:n.411G>C (STRC)
ENST00000471703.5:n.2786G>C (STRC)
ENST00000485556.5:n.3687G>C (STRC)
ENST00000541030.5:c.2513G>C (STRC)	ENSP00000440413.1:p.Ser838Thr
NM_153700.2:c.4832G>C (STRC) MANE Select	NP_714544.1:p.Ser1611Thr
XM_011521277.1:c.5321G>C (STRC)	XP_011519579.1:p.Ser1774Thr
XM_011521278.1:c.4937G>C (STRC)	XP_011519580.1:p.Ser1646Thr
XM_011521279.1:c.4937G>C (STRC)	XP_011519581.1:p.Ser1646Thr