Canonical Allele Identifier: CA363264194

Gene: CDKAL1

Linked Data

• MyVariant Identifiers: chr6:g.20546708A>G (hg19) ; chr6:g.20546477A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20546477A>G , CM000668.2:g.20546477A>G	GRCh38
NC_000006.11:g.20546708A>G , CM000668.1:g.20546708A>G	GRCh37
NC_000006.10:g.20654687A>G	NCBI36
NG_021195.1:g.17021A>G
NG_021195.2:g.17021A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000274695.8:c.127A>G MANE Select	ENSP00000274695.4:p.Thr43Ala
ENST00000378610.1:c.127A>G	ENSP00000367873.1:p.Thr43Ala
ENST00000613575.4:c.127A>G	ENSP00000481755.1:p.Thr43Ala
NM_017774.3:c.127A>G MANE Select	NP_060244.2:p.Thr43Ala
XM_006715128.2:c.127A>G	XP_006715191.1:p.Thr43Ala
XM_011514718.1:c.127A>G	XP_011513020.1:p.Thr43Ala
XM_011514719.1:c.127A>G	XP_011513021.1:p.Thr43Ala
XR_926265.1:n.294A>G
XR_926266.1:n.407A>G
XR_926267.1:n.294A>G
XM_011514719.2:c.127A>G	XP_011513021.1:p.Thr43Ala
XM_017010986.1:c.127A>G	XP_016866475.1:p.Thr43Ala
XM_017010987.1:c.-628A>G	XP_016866476.1:n.-628A>G
XM_024446481.1:c.127A>G	XP_024302249.1:p.Thr43Ala
XR_001743495.2:n.299A>G
XR_001743496.2:n.694A>G
XR_001743500.1:n.294A>G
XR_001743501.1:n.294A>G
XR_926265.2:n.294A>G
XR_926266.2:n.407A>G
XR_926267.2:n.294A>G