Canonical Allele Identifier: CA392157570

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43891913C>G (hg19) ; chr15:g.43599715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599715C>G , CM000677.2:g.43599715C>G	GRCh38
NC_000015.9:g.43891913C>G , CM000677.1:g.43891913C>G	GRCh37
NC_000015.8:g.41679205C>G	NCBI36
NG_011636.1:g.24086G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5285G>C (STRC) MANE Select	ENSP00000401513.2:p.Trp1762Ser
ENST00000411560.1:n.142+182C>G (CKMT1B)
ENST00000428650.5:c.*2318G>C (STRC)	ENSP00000415991.1:n.*2318G>C
ENST00000440125.5:c.*3077G>C (STRC)	ENSP00000394866.1:n.*3077G>C
ENST00000448437.6:n.2405G>C (STRC)
ENST00000450892.6:c.5285G>C (STRC)	ENSP00000401513.2:p.Trp1762Ser
ENST00000471703.5:n.3239G>C (STRC)
ENST00000485556.5:n.4140G>C (STRC)
ENST00000541030.5:c.2966G>C (STRC)	ENSP00000440413.1:p.Trp989Ser
NM_153700.2:c.5285G>C (STRC) MANE Select	NP_714544.1:p.Trp1762Ser
XM_011521277.1:c.5774G>C (STRC)	XP_011519579.1:p.Trp1925Ser
XM_011521278.1:c.5390G>C (STRC)	XP_011519580.1:p.Trp1797Ser
XM_011521279.1:c.5390G>C (STRC)	XP_011519581.1:p.Trp1797Ser