Canonical Allele Identifier: CA135729700

Gene: CDKAL1

Linked Data

• dbSNP Id: rs1045351494
• gnomAD v3: 6-20856554-TAAC-T
• gnomAD v4: 6-20856554-TAAC-T
• MyVariant Identifiers: chr6:g.20856786_20856788del (hg19) ; chr6:g.20856555_20856557del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20856555_20856557del , CM000668.2:g.20856555_20856557del	GRCh38
NC_000006.11:g.20856786_20856788del , CM000668.1:g.20856786_20856788del	GRCh37
NC_000006.10:g.20964765_20964767del	NCBI36
NG_021195.1:g.327099_327101del
NG_021195.2:g.327099_327101del

Transcript Alleles

HGVS	Amino-acid change
ENST00000274695.8:c.742+10377_742+10379del MANE Select	ENSP00000274695.4:n.742+10377_742+10379de...
ENST00000378610.1:c.742+10377_742+10379del	ENSP00000367873.1:n.742+10377_742+10379de...
NM_017774.3:c.742+10377_742+10379del MANE Select	NP_060244.2:n.742+10377_742+10379del
XM_006715128.2:c.742+10377_742+10379del	XP_006715191.1:n.742+10377_742+10379del
XM_011514718.1:c.742+10377_742+10379del	XP_011513020.1:n.742+10377_742+10379del
XM_011514719.1:c.742+10377_742+10379del	XP_011513021.1:n.742+10377_742+10379del
XR_926265.1:n.909+10377_909+10379del
XR_926266.1:n.1022+10377_1022+10379del
XR_926267.1:n.909+10377_909+10379del
XM_011514719.2:c.742+10377_742+10379del	XP_011513021.1:n.742+10377_742+10379del
XM_017010986.1:c.742+10377_742+10379del	XP_016866475.1:n.742+10377_742+10379del
XM_017010987.1:c.-117+75290_-117+75292del	XP_016866476.1:n.-117+75290_-117+75292del...
XM_024446481.1:c.742+10377_742+10379del	XP_024302249.1:n.742+10377_742+10379del
XR_001743495.2:n.914+10377_914+10379del
XR_001743496.2:n.1309+10377_1309+10379del
XR_001743498.2:n.2641+10377_2641+10379del
XR_001743500.1:n.909+10377_909+10379del
XR_001743501.1:n.909+10377_909+10379del
XR_926265.2:n.909+10377_909+10379del
XR_926266.2:n.1022+10377_1022+10379del
XR_926267.2:n.909+10377_909+10379del