Canonical Allele Identifier: CA392157957

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892169G>C (hg19) ; chr15:g.43599971G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599971G>C , CM000677.2:g.43599971G>C	GRCh38
NC_000015.9:g.43892169G>C , CM000677.1:g.43892169G>C	GRCh37
NC_000015.8:g.41679461G>C	NCBI36
NG_011636.1:g.23830C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5228C>G (STRC) MANE Select	ENSP00000401513.2:p.Pro1743Arg
ENST00000411560.1:n.142+438G>C (CKMT1B)
ENST00000428650.5:c.*2261C>G (STRC)	ENSP00000415991.1:n.*2261C>G
ENST00000440125.5:c.*3020C>G (STRC)	ENSP00000394866.1:n.*3020C>G
ENST00000448437.6:n.2348C>G (STRC)
ENST00000450892.6:c.5228C>G (STRC)	ENSP00000401513.2:p.Pro1743Arg
ENST00000471703.5:n.3182C>G (STRC)
ENST00000485556.5:n.4083C>G (STRC)
ENST00000541030.5:c.2909C>G (STRC)	ENSP00000440413.1:p.Pro970Arg
NM_153700.2:c.5228C>G (STRC) MANE Select	NP_714544.1:p.Pro1743Arg
XM_011521277.1:c.5717C>G (STRC)	XP_011519579.1:p.Pro1906Arg
XM_011521278.1:c.5333C>G (STRC)	XP_011519580.1:p.Pro1778Arg
XM_011521279.1:c.5333C>G (STRC)	XP_011519581.1:p.Pro1778Arg