Canonical Allele Identifier: CA822973565

Gene: CDKAL1

Linked Data

• dbSNP Id: rs1383406511
• gnomAD v3: 6-20678109-T-C
• gnomAD v4: 6-20678109-T-C
• MyVariant Identifiers: chr6:g.20678340T>C (hg19) ; chr6:g.20678109T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20678109T>C , CM000668.2:g.20678109T>C	GRCh38
NC_000006.11:g.20678340T>C , CM000668.1:g.20678340T>C	GRCh37
NC_000006.10:g.20786319T>C	NCBI36
NG_021195.1:g.148653T>C
NG_021195.2:g.148653T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274695.8:c.371+28732T>C MANE Select	ENSP00000274695.4:n.371+28732T>C
ENST00000378610.1:c.371+28732T>C	ENSP00000367873.1:n.371+28732T>C
NM_017774.3:c.371+28732T>C MANE Select	NP_060244.2:n.371+28732T>C
XM_006715128.2:c.371+28732T>C	XP_006715191.1:n.371+28732T>C
XM_011514718.1:c.371+28732T>C	XP_011513020.1:n.371+28732T>C
XM_011514719.1:c.371+28732T>C	XP_011513021.1:n.371+28732T>C
XR_926265.1:n.538+28732T>C
XR_926266.1:n.651+28732T>C
XR_926267.1:n.538+28732T>C
XM_011514719.2:c.371+28732T>C	XP_011513021.1:n.371+28732T>C
XM_017010986.1:c.371+28732T>C	XP_016866475.1:n.371+28732T>C
XM_017010987.1:c.-384+28732T>C	XP_016866476.1:n.-384+28732T>C
XM_024446481.1:c.371+28732T>C	XP_024302249.1:n.371+28732T>C
XR_001743495.2:n.543+28732T>C
XR_001743496.2:n.938+28732T>C
XR_001743500.1:n.538+28732T>C
XR_001743501.1:n.538+28732T>C
XR_926265.2:n.538+28732T>C
XR_926266.2:n.651+28732T>C
XR_926267.2:n.538+28732T>C