Canonical Allele Identifier: CA392158001

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892175T>G (hg19) ; chr15:g.43599977T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599977T>G , CM000677.2:g.43599977T>G	GRCh38
NC_000015.9:g.43892175T>G , CM000677.1:g.43892175T>G	GRCh37
NC_000015.8:g.41679467T>G	NCBI36
NG_011636.1:g.23824A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5222A>C (STRC) MANE Select	ENSP00000401513.2:p.Glu1741Ala
ENST00000411560.1:n.142+444T>G (CKMT1B)
ENST00000428650.5:c.*2255A>C (STRC)	ENSP00000415991.1:n.*2255A>C
ENST00000440125.5:c.*3014A>C (STRC)	ENSP00000394866.1:n.*3014A>C
ENST00000448437.6:n.2342A>C (STRC)
ENST00000450892.6:c.5222A>C (STRC)	ENSP00000401513.2:p.Glu1741Ala
ENST00000471703.5:n.3176A>C (STRC)
ENST00000485556.5:n.4077A>C (STRC)
ENST00000541030.5:c.2903A>C (STRC)	ENSP00000440413.1:p.Glu968Ala
NM_153700.2:c.5222A>C (STRC) MANE Select	NP_714544.1:p.Glu1741Ala
XM_011521277.1:c.5711A>C (STRC)	XP_011519579.1:p.Glu1904Ala
XM_011521278.1:c.5327A>C (STRC)	XP_011519580.1:p.Glu1776Ala
XM_011521279.1:c.5327A>C (STRC)	XP_011519581.1:p.Glu1776Ala