Canonical Allele Identifier: CA618004400

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs1359282599
• gnomAD v2: 15-43893756-G-A
• gnomAD v4: 15-43601558-G-A
• MyVariant Identifiers: chr15:g.43893756G>A (hg19) ; chr15:g.43601558G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601558G>A , CM000677.2:g.43601558G>A	GRCh38
NC_000015.9:g.43893756G>A , CM000677.1:g.43893756G>A	GRCh37
NC_000015.8:g.41681048G>A	NCBI36
NG_011636.1:g.22243C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4546-7C>T (STRC) MANE Select	ENSP00000401513.2:n.4546-7C>T
ENST00000411560.1:n.142+2025G>A (CKMT1B)
ENST00000428650.5:c.*1579-7C>T (STRC)	ENSP00000415991.1:n.*1579-7C>T
ENST00000440125.5:c.*2338-7C>T (STRC)	ENSP00000394866.1:n.*2338-7C>T
ENST00000448437.6:n.1666-7C>T (STRC)
ENST00000450892.6:c.4546-7C>T (STRC)	ENSP00000401513.2:n.4546-7C>T
ENST00000460952.1:n.118C>T (STRC)
ENST00000471703.5:n.2500-7C>T (STRC)
ENST00000485556.5:n.3401-7C>T (STRC)
ENST00000493750.1:n.342-7C>T (STRC)
ENST00000541030.5:c.2227-7C>T (STRC)	ENSP00000440413.1:n.2227-7C>T
NM_153700.2:c.4546-7C>T (STRC) MANE Select	NP_714544.1:n.4546-7C>T
XM_011521277.1:c.5035-7C>T (STRC)	XP_011519579.1:n.5035-7C>T
XM_011521278.1:c.4651-7C>T (STRC)	XP_011519580.1:n.4651-7C>T
XM_011521279.1:c.4651-7C>T (STRC)	XP_011519581.1:n.4651-7C>T