Canonical Allele Identifier: CA392160055

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43600560-A-T
• MyVariant Identifiers: chr15:g.43892758A>T (hg19) ; chr15:g.43600560A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600560A>T , CM000677.2:g.43600560A>T	GRCh38
NC_000015.9:g.43892758A>T , CM000677.1:g.43892758A>T	GRCh37
NC_000015.8:g.41680050A>T	NCBI36
NG_011636.1:g.23241T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4967T>A (STRC) MANE Select	ENSP00000401513.2:p.Ile1656Asn
ENST00000411560.1:n.142+1027A>T (CKMT1B)
ENST00000428650.5:c.*2000T>A (STRC)	ENSP00000415991.1:n.*2000T>A
ENST00000440125.5:c.*2759T>A (STRC)	ENSP00000394866.1:n.*2759T>A
ENST00000448437.6:n.2087T>A (STRC)
ENST00000450892.6:c.4967T>A (STRC)	ENSP00000401513.2:p.Ile1656Asn
ENST00000471703.5:n.2921T>A (STRC)
ENST00000485556.5:n.3822T>A (STRC)
ENST00000541030.5:c.2648T>A (STRC)	ENSP00000440413.1:p.Ile883Asn
NM_153700.2:c.4967T>A (STRC) MANE Select	NP_714544.1:p.Ile1656Asn
XM_011521277.1:c.5456T>A (STRC)	XP_011519579.1:p.Ile1819Asn
XM_011521278.1:c.5072T>A (STRC)	XP_011519580.1:p.Ile1691Asn
XM_011521279.1:c.5072T>A (STRC)	XP_011519581.1:p.Ile1691Asn