Canonical Allele Identifier: CA392157914

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892162C>A (hg19) ; chr15:g.43599964C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599964C>A , CM000677.2:g.43599964C>A	GRCh38
NC_000015.9:g.43892162C>A , CM000677.1:g.43892162C>A	GRCh37
NC_000015.8:g.41679454C>A	NCBI36
NG_011636.1:g.23837G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5235G>T (STRC) MANE Select	ENSP00000401513.2:p.Gln1745His
ENST00000411560.1:n.142+431C>A (CKMT1B)
ENST00000428650.5:c.*2268G>T (STRC)	ENSP00000415991.1:n.*2268G>T
ENST00000440125.5:c.*3027G>T (STRC)	ENSP00000394866.1:n.*3027G>T
ENST00000448437.6:n.2355G>T (STRC)
ENST00000450892.6:c.5235G>T (STRC)	ENSP00000401513.2:p.Gln1745His
ENST00000471703.5:n.3189G>T (STRC)
ENST00000485556.5:n.4090G>T (STRC)
ENST00000541030.5:c.2916G>T (STRC)	ENSP00000440413.1:p.Gln972His
NM_153700.2:c.5235G>T (STRC) MANE Select	NP_714544.1:p.Gln1745His
XM_011521277.1:c.5724G>T (STRC)	XP_011519579.1:p.Gln1908His
XM_011521278.1:c.5340G>T (STRC)	XP_011519580.1:p.Gln1780His
XM_011521279.1:c.5340G>T (STRC)	XP_011519581.1:p.Gln1780His