Canonical Allele Identifier: CA490145038

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43600886-G-A
• MyVariant Identifiers: chr15:g.43893084G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600886G>A , CM000677.2:g.43600886G>A	GRCh38
NC_000015.9:g.43893084G>A , CM000677.1:g.43893084G>A	GRCh37
NC_000015.8:g.41680376G>A	NCBI36
NG_011636.1:g.22915C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4830C>T (STRC) MANE Select	ENSP00000401513.2:p.Ser1610=
ENST00000411560.1:n.142+1353G>A (CKMT1B)
ENST00000428650.5:c.*1863C>T (STRC)	ENSP00000415991.1:n.*1863C>T
ENST00000440125.5:c.*2622C>T (STRC)	ENSP00000394866.1:n.*2622C>T
ENST00000448437.6:n.1950C>T (STRC)
ENST00000450892.6:c.4830C>T (STRC)	ENSP00000401513.2:p.Ser1610=
ENST00000460952.1:n.409C>T (STRC)
ENST00000471703.5:n.2784C>T (STRC)
ENST00000485556.5:n.3685C>T (STRC)
ENST00000541030.5:c.2511C>T (STRC)	ENSP00000440413.1:p.Ser837=
NM_153700.2:c.4830C>T (STRC) MANE Select	NP_714544.1:p.Ser1610=
XM_011521277.1:c.5319C>T (STRC)	XP_011519579.1:p.Ser1773=
XM_011521278.1:c.4935C>T (STRC)	XP_011519580.1:p.Ser1645=
XM_011521279.1:c.4935C>T (STRC)	XP_011519581.1:p.Ser1645=