Canonical Allele Identifier: CA618004428

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs1192669491
• gnomAD v2: 15-43896552-A-G
• gnomAD v4: 15-43604354-A-G
• MyVariant Identifiers: chr15:g.43896552A>G (hg19) ; chr15:g.43604354A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604354A>G , CM000677.2:g.43604354A>G	GRCh38
NC_000015.9:g.43896552A>G , CM000677.1:g.43896552A>G	GRCh37
NC_000015.8:g.41683844A>G	NCBI36
NG_011636.1:g.19447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4218+7T>C (STRC) MANE Select	ENSP00000401513.2:n.4218+7T>C
ENST00000411560.1:n.143-430A>G (CKMT1B)
ENST00000428650.5:c.*1421+7T>C (STRC)	ENSP00000415991.1:n.*1421+7T>C
ENST00000440125.5:c.*2010+7T>C (STRC)	ENSP00000394866.1:n.*2010+7T>C
ENST00000448437.6:n.1666-2803T>C (STRC)
ENST00000450892.6:c.4218+7T>C (STRC)	ENSP00000401513.2:n.4218+7T>C
ENST00000471703.5:n.2172+7T>C (STRC)
ENST00000485556.5:n.3073+7T>C (STRC)
ENST00000541030.5:c.1899+7T>C (STRC)	ENSP00000440413.1:n.1899+7T>C
NM_153700.2:c.4218+7T>C (STRC) MANE Select	NP_714544.1:n.4218+7T>C
XM_011521277.1:c.4707+7T>C (STRC)	XP_011519579.1:n.4707+7T>C
XM_011521278.1:c.4323+7T>C (STRC)	XP_011519580.1:n.4323+7T>C
XM_011521279.1:c.4323+7T>C (STRC)	XP_011519581.1:n.4323+7T>C