Canonical Allele Identifier: CA822973619

Gene: CDKAL1

Linked Data

• dbSNP Id: rs1302013768
• MyVariant Identifiers: chr6:g.20678493_20678495del (hg19) ; chr6:g.20678262_20678264del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20678262_20678264del , CM000668.2:g.20678262_20678264del	GRCh38
NC_000006.11:g.20678493_20678495del , CM000668.1:g.20678493_20678495del	GRCh37
NC_000006.10:g.20786472_20786474del	NCBI36
NG_021195.1:g.148806_148808del
NG_021195.2:g.148806_148808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274695.8:c.371+28885_371+28887del MANE Select	ENSP00000274695.4:n.371+28885_371+28887del
ENST00000378610.1:c.371+28885_371+28887del	ENSP00000367873.1:n.371+28885_371+28887del
NM_017774.3:c.371+28885_371+28887del MANE Select	NP_060244.2:n.371+28885_371+28887del
XM_006715128.2:c.371+28885_371+28887del	XP_006715191.1:n.371+28885_371+28887del
XM_011514718.1:c.371+28885_371+28887del	XP_011513020.1:n.371+28885_371+28887del
XM_011514719.1:c.371+28885_371+28887del	XP_011513021.1:n.371+28885_371+28887del
XR_926265.1:n.538+28885_538+28887del
XR_926266.1:n.651+28885_651+28887del
XR_926267.1:n.538+28885_538+28887del
XM_011514719.2:c.371+28885_371+28887del	XP_011513021.1:n.371+28885_371+28887del
XM_017010986.1:c.371+28885_371+28887del	XP_016866475.1:n.371+28885_371+28887del
XM_017010987.1:c.-384+28885_-384+28887del	XP_016866476.1:n.-384+28885_-384+28887del
XM_024446481.1:c.371+28885_371+28887del	XP_024302249.1:n.371+28885_371+28887del
XR_001743495.2:n.543+28885_543+28887del
XR_001743496.2:n.938+28885_938+28887del
XR_001743500.1:n.538+28885_538+28887del
XR_001743501.1:n.538+28885_538+28887del
XR_926265.2:n.538+28885_538+28887del
XR_926266.2:n.651+28885_651+28887del
XR_926267.2:n.538+28885_538+28887del