Canonical Allele Identifier: CA490144672

Gene: STRC CKMT1B

Linked Data

• COSMIC: COSM234119
• MyVariant Identifiers: chr15:g.43892724C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600526C>T , CM000677.2:g.43600526C>T	GRCh38
NC_000015.9:g.43892724C>T , CM000677.1:g.43892724C>T	GRCh37
NC_000015.8:g.41680016C>T	NCBI36
NG_011636.1:g.23275G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4993+8G>A (STRC) MANE Select	ENSP00000401513.2:n.4993+8G>A
ENST00000411560.1:n.142+993C>T (CKMT1B)
ENST00000428650.5:c.*2026+8G>A (STRC)	ENSP00000415991.1:n.*2026+8G>A
ENST00000440125.5:c.*2785+8G>A (STRC)	ENSP00000394866.1:n.*2785+8G>A
ENST00000448437.6:n.2113+8G>A (STRC)
ENST00000450892.6:c.4993+8G>A (STRC)	ENSP00000401513.2:n.4993+8G>A
ENST00000471703.5:n.2947+8G>A (STRC)
ENST00000485556.5:n.3848+8G>A (STRC)
ENST00000541030.5:c.2674+8G>A (STRC)	ENSP00000440413.1:n.2674+8G>A
NM_153700.2:c.4993+8G>A (STRC) MANE Select	NP_714544.1:n.4993+8G>A
XM_011521277.1:c.5482+8G>A (STRC)	XP_011519579.1:n.5482+8G>A
XM_011521278.1:c.5098+8G>A (STRC)	XP_011519580.1:n.5098+8G>A
XM_011521279.1:c.5098+8G>A (STRC)	XP_011519581.1:n.5098+8G>A