Canonical Allele Identifier: CA392167845

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43896568C>A (hg19) ; chr15:g.43604370C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604370C>A , CM000677.2:g.43604370C>A	GRCh38
NC_000015.9:g.43896568C>A , CM000677.1:g.43896568C>A	GRCh37
NC_000015.8:g.41683860C>A	NCBI36
NG_011636.1:g.19431G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4209G>T (STRC) MANE Select	ENSP00000401513.2:p.Leu1403Phe
ENST00000411560.1:n.143-414C>A (CKMT1B)
ENST00000428650.5:c.*1412G>T (STRC)	ENSP00000415991.1:n.*1412G>T
ENST00000440125.5:c.*2001G>T (STRC)	ENSP00000394866.1:n.*2001G>T
ENST00000448437.6:n.1666-2819G>T (STRC)
ENST00000450892.6:c.4209G>T (STRC)	ENSP00000401513.2:p.Leu1403Phe
ENST00000471703.5:n.2163G>T (STRC)
ENST00000485556.5:n.3064G>T (STRC)
ENST00000541030.5:c.1890G>T (STRC)	ENSP00000440413.1:p.Leu630Phe
NM_153700.2:c.4209G>T (STRC) MANE Select	NP_714544.1:p.Leu1403Phe
XM_011521277.1:c.4698G>T (STRC)	XP_011519579.1:p.Leu1566Phe
XM_011521278.1:c.4314G>T (STRC)	XP_011519580.1:p.Leu1438Phe
XM_011521279.1:c.4314G>T (STRC)	XP_011519581.1:p.Leu1438Phe