Canonical Allele Identifier: CA363264198

Gene: CDKAL1

Linked Data

• dbSNP Id: rs1763608746
• MyVariant Identifiers: chr6:g.20546709C>T (hg19) ; chr6:g.20546478C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20546478C>T , CM000668.2:g.20546478C>T	GRCh38
NC_000006.11:g.20546709C>T , CM000668.1:g.20546709C>T	GRCh37
NC_000006.10:g.20654688C>T	NCBI36
NG_021195.1:g.17022C>T
NG_021195.2:g.17022C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000274695.8:c.128C>T MANE Select	ENSP00000274695.4:p.Thr43Ile
ENST00000378610.1:c.128C>T	ENSP00000367873.1:p.Thr43Ile
ENST00000613575.4:c.128C>T	ENSP00000481755.1:p.Thr43Ile
NM_017774.3:c.128C>T MANE Select	NP_060244.2:p.Thr43Ile
XM_006715128.2:c.128C>T	XP_006715191.1:p.Thr43Ile
XM_011514718.1:c.128C>T	XP_011513020.1:p.Thr43Ile
XM_011514719.1:c.128C>T	XP_011513021.1:p.Thr43Ile
XR_926265.1:n.295C>T
XR_926266.1:n.408C>T
XR_926267.1:n.295C>T
XM_011514719.2:c.128C>T	XP_011513021.1:p.Thr43Ile
XM_017010986.1:c.128C>T	XP_016866475.1:p.Thr43Ile
XM_017010987.1:c.-627C>T	XP_016866476.1:n.-627C>T
XM_024446481.1:c.128C>T	XP_024302249.1:p.Thr43Ile
XR_001743495.2:n.300C>T
XR_001743496.2:n.695C>T
XR_001743500.1:n.295C>T
XR_001743501.1:n.295C>T
XR_926265.2:n.295C>T
XR_926266.2:n.408C>T
XR_926267.2:n.295C>T