Canonical Allele Identifier: CA566063467

Gene: CDKAL1

Linked Data

• gnomAD v2: 6-20678336-A-ATTTT
• gnomAD v3: 6-20678105-A-ATTTT
• gnomAD v4: 6-20678105-A-ATTTT
• MyVariant Identifiers: chr6:g.20678337_20678338delinsTTTTCT (hg19) ; chr6:g.20678106_20678107delinsTTTTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20678105_20678106insTTTT , CM000668.2:g.20678105_20678106insTTTT	GRCh38
NC_000006.11:g.20678336_20678337insTTTT , CM000668.1:g.20678336_20678337insTTTT	GRCh37
NC_000006.10:g.20786315_20786316insTTTT	NCBI36
NG_021195.1:g.148649_148650insTTTT
NG_021195.2:g.148649_148650insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274695.8:c.371+28728_371+28729insTTTT MANE Select	ENSP00000274695.4:n.371+28728_371+28729insTTTT
ENST00000378610.1:c.371+28728_371+28729insTTTT	ENSP00000367873.1:n.371+28728_371+28729insTTTT
NM_017774.3:c.371+28728_371+28729insTTTT MANE Select	NP_060244.2:n.371+28728_371+28729insTTTT
XM_006715128.2:c.371+28728_371+28729insTTTT	XP_006715191.1:n.371+28728_371+28729insTTTT
XM_011514718.1:c.371+28728_371+28729insTTTT	XP_011513020.1:n.371+28728_371+28729insTTTT
XM_011514719.1:c.371+28728_371+28729insTTTT	XP_011513021.1:n.371+28728_371+28729insTTTT
XR_926265.1:n.538+28728_538+28729insTTTT
XR_926266.1:n.651+28728_651+28729insTTTT
XR_926267.1:n.538+28728_538+28729insTTTT
XM_011514719.2:c.371+28728_371+28729insTTTT	XP_011513021.1:n.371+28728_371+28729insTTTT
XM_017010986.1:c.371+28728_371+28729insTTTT	XP_016866475.1:n.371+28728_371+28729insTTTT
XM_017010987.1:c.-384+28728_-384+28729insTTTT	XP_016866476.1:n.-384+28728_-384+28729insTTTT
XM_024446481.1:c.371+28728_371+28729insTTTT	XP_024302249.1:n.371+28728_371+28729insTTTT
XR_001743495.2:n.543+28728_543+28729insTTTT
XR_001743496.2:n.938+28728_938+28729insTTTT
XR_001743500.1:n.538+28728_538+28729insTTTT
XR_001743501.1:n.538+28728_538+28729insTTTT
XR_926265.2:n.538+28728_538+28729insTTTT
XR_926266.2:n.651+28728_651+28729insTTTT
XR_926267.2:n.538+28728_538+28729insTTTT