Canonical Allele Identifier: CA7527772

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs575443944
• ExAC: 15:43892126 T / C
• gnomAD v2: 15-43892126-T-C
• gnomAD v3: 15-43599928-T-C
• gnomAD v4: 15-43599928-T-C
• MyVariant Identifiers: chr15:g.43892126T>C (hg19) ; chr15:g.43599928T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599928T>C , CM000677.2:g.43599928T>C	GRCh38
NC_000015.9:g.43892126T>C , CM000677.1:g.43892126T>C	GRCh37
NC_000015.8:g.41679418T>C	NCBI36
NG_011636.1:g.23873A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5239+32A>G (STRC) MANE Select	ENSP00000401513.2:n.5239+32A>G
ENST00000411560.1:n.142+395T>C (CKMT1B)
ENST00000428650.5:c.*2272+32A>G (STRC)	ENSP00000415991.1:n.*2272+32A>G
ENST00000440125.5:c.*3031+32A>G (STRC)	ENSP00000394866.1:n.*3031+32A>G
ENST00000448437.6:n.2359+32A>G (STRC)
ENST00000450892.6:c.5239+32A>G (STRC)	ENSP00000401513.2:n.5239+32A>G
ENST00000471703.5:n.3193+32A>G (STRC)
ENST00000485556.5:n.4094+32A>G (STRC)
ENST00000541030.5:c.2920+32A>G (STRC)	ENSP00000440413.1:n.2920+32A>G
NM_153700.2:c.5239+32A>G (STRC) MANE Select	NP_714544.1:n.5239+32A>G
XM_011521277.1:c.5728+32A>G (STRC)	XP_011519579.1:n.5728+32A>G
XM_011521278.1:c.5344+32A>G (STRC)	XP_011519580.1:n.5344+32A>G
XM_011521279.1:c.5344+32A>G (STRC)	XP_011519581.1:n.5344+32A>G