Canonical Allele Identifier: CA566063916

Gene: CDKAL1

Linked Data

• dbSNP Id: rs1203638211
• gnomAD v2: 6-20679588-A-T
• gnomAD v3: 6-20679357-A-T
• gnomAD v4: 6-20679357-A-T
• MyVariant Identifiers: chr6:g.20679588A>T (hg19) ; chr6:g.20679357A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20679357A>T , CM000668.2:g.20679357A>T	GRCh38
NC_000006.11:g.20679588A>T , CM000668.1:g.20679588A>T	GRCh37
NC_000006.10:g.20787567A>T	NCBI36
NG_021195.1:g.149901A>T
NG_021195.2:g.149901A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000274695.8:c.371+29980A>T MANE Select	ENSP00000274695.4:n.371+29980A>T
ENST00000378610.1:c.371+29980A>T	ENSP00000367873.1:n.371+29980A>T
NM_017774.3:c.371+29980A>T MANE Select	NP_060244.2:n.371+29980A>T
XM_006715128.2:c.371+29980A>T	XP_006715191.1:n.371+29980A>T
XM_011514718.1:c.371+29980A>T	XP_011513020.1:n.371+29980A>T
XM_011514719.1:c.371+29980A>T	XP_011513021.1:n.371+29980A>T
XR_926265.1:n.538+29980A>T
XR_926266.1:n.651+29980A>T
XR_926267.1:n.538+29980A>T
XM_011514719.2:c.371+29980A>T	XP_011513021.1:n.371+29980A>T
XM_017010986.1:c.371+29980A>T	XP_016866475.1:n.371+29980A>T
XM_017010987.1:c.-384+29980A>T	XP_016866476.1:n.-384+29980A>T
XM_024446481.1:c.371+29980A>T	XP_024302249.1:n.371+29980A>T
XR_001743495.2:n.543+29980A>T
XR_001743496.2:n.938+29980A>T
XR_001743500.1:n.538+29980A>T
XR_001743501.1:n.538+29980A>T
XR_926265.2:n.538+29980A>T
XR_926266.2:n.651+29980A>T
XR_926267.2:n.538+29980A>T