Canonical Allele Identifier: CA392168749

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43896921G>T (hg19) ; chr15:g.43604723G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604723G>T , CM000677.2:g.43604723G>T	GRCh38
NC_000015.9:g.43896921G>T , CM000677.1:g.43896921G>T	GRCh37
NC_000015.8:g.41684213G>T	NCBI36
NG_011636.1:g.19078C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4054C>A (STRC) MANE Select	ENSP00000401513.2:p.Leu1352Met
ENST00000411560.1:n.143-61G>T (CKMT1B)
ENST00000428650.5:c.*1257C>A (STRC)	ENSP00000415991.1:n.*1257C>A
ENST00000440125.5:c.*1846C>A (STRC)	ENSP00000394866.1:n.*1846C>A
ENST00000448437.6:n.1665+3140C>A (STRC)
ENST00000450892.6:c.4054C>A (STRC)	ENSP00000401513.2:p.Leu1352Met
ENST00000455136.5:c.1085C>A (STRC)
ENST00000471703.5:n.2008C>A (STRC)
ENST00000485556.5:n.2909C>A (STRC)
ENST00000541030.5:c.1735C>A (STRC)	ENSP00000440413.1:p.Leu579Met
NM_153700.2:c.4054C>A (STRC) MANE Select	NP_714544.1:p.Leu1352Met
XM_011521277.1:c.4543C>A (STRC)	XP_011519579.1:p.Leu1515Met
XM_011521278.1:c.4159C>A (STRC)	XP_011519580.1:p.Leu1387Met
XM_011521279.1:c.4159C>A (STRC)	XP_011519581.1:p.Leu1387Met