Canonical Allele Identifier: CA392157877

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43599960-C-T
• MyVariant Identifiers: chr15:g.43892158C>T (hg19) ; chr15:g.43599960C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599960C>T , CM000677.2:g.43599960C>T	GRCh38
NC_000015.9:g.43892158C>T , CM000677.1:g.43892158C>T	GRCh37
NC_000015.8:g.41679450C>T	NCBI36
NG_011636.1:g.23841G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5239G>A (STRC) MANE Select	ENSP00000401513.2:p.Gly1747Ser
ENST00000411560.1:n.142+427C>T (CKMT1B)
ENST00000428650.5:c.*2272G>A (STRC)	ENSP00000415991.1:n.*2272G>A
ENST00000440125.5:c.*3031G>A (STRC)	ENSP00000394866.1:n.*3031G>A
ENST00000448437.6:n.2359G>A (STRC)
ENST00000450892.6:c.5239G>A (STRC)	ENSP00000401513.2:p.Gly1747Ser
ENST00000471703.5:n.3193G>A (STRC)
ENST00000485556.5:n.4094G>A (STRC)
ENST00000541030.5:c.2920G>A (STRC)	ENSP00000440413.1:p.Gly974Ser
NM_153700.2:c.5239G>A (STRC) MANE Select	NP_714544.1:p.Gly1747Ser
XM_011521277.1:c.5728G>A (STRC)	XP_011519579.1:p.Gly1910Ser
XM_011521278.1:c.5344G>A (STRC)	XP_011519580.1:p.Gly1782Ser
XM_011521279.1:c.5344G>A (STRC)	XP_011519581.1:p.Gly1782Ser