Canonical Allele Identifier: CA618004296

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs1475564721
• gnomAD v2: 15-43891841-C-T
• gnomAD v4: 15-43599643-C-T
• MyVariant Identifiers: chr15:g.43891841C>T (hg19) ; chr15:g.43599643C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599643C>T , CM000677.2:g.43599643C>T	GRCh38
NC_000015.9:g.43891841C>T , CM000677.1:g.43891841C>T	GRCh37
NC_000015.8:g.41679133C>T	NCBI36
NG_011636.1:g.24158G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.*29G>A (STRC) MANE Select	ENSP00000401513.2:n.*29G>A
ENST00000411560.1:n.142+110C>T (CKMT1B)
ENST00000428650.5:c.*2390G>A (STRC)	ENSP00000415991.1:n.*2390G>A
ENST00000440125.5:c.*3149G>A (STRC)	ENSP00000394866.1:n.*3149G>A
ENST00000448437.6:n.2477G>A (STRC)
ENST00000450892.6:c.*29G>A (STRC)	ENSP00000401513.2:n.*29G>A
ENST00000471703.5:n.3311G>A (STRC)
ENST00000485556.5:n.4212G>A (STRC)
ENST00000541030.5:c.*29G>A (STRC)	ENSP00000440413.1:n.*29G>A
NM_153700.2:c.*29G>A (STRC) MANE Select	NP_714544.1:n.*29G>A
XM_011521277.1:c.*29G>A (STRC)	XP_011519579.1:n.*29G>A
XM_011521278.1:c.*29G>A (STRC)	XP_011519580.1:n.*29G>A
XM_011521279.1:c.*29G>A (STRC)	XP_011519581.1:n.*29G>A