Canonical Allele Identifier: CA1614687602
Gene: CDKAL1 HGNC NCBI

Linked Data

dbSNP Id: rs1768810907

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.20652347G>T , CM000668.2:g.20652347G>T GRCh38
NC_000006.11:g.20652578G>T , CM000668.1:g.20652578G>T GRCh37
NC_000006.10:g.20760557G>T NCBI36
NG_021195.1:g.122891G>T
NG_021195.2:g.122891G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274695.8:c.371+2970G>T MANE Select ENSP00000274695.4:n.371+2970G>T
ENST00000378610.1:c.371+2970G>T ENSP00000367873.1:n.371+2970G>T
NM_017774.3:c.371+2970G>T MANE Select NP_060244.2:n.371+2970G>T
XM_006715128.2:c.371+2970G>T XP_006715191.1:n.371+2970G>T
XM_011514718.1:c.371+2970G>T XP_011513020.1:n.371+2970G>T
XM_011514719.1:c.371+2970G>T XP_011513021.1:n.371+2970G>T
XR_926265.1:n.538+2970G>T
XR_926266.1:n.651+2970G>T
XR_926267.1:n.538+2970G>T
XM_011514719.2:c.371+2970G>T XP_011513021.1:n.371+2970G>T
XM_017010986.1:c.371+2970G>T XP_016866475.1:n.371+2970G>T
XM_017010987.1:c.-384+2970G>T XP_016866476.1:n.-384+2970G>T
XM_024446481.1:c.371+2970G>T XP_024302249.1:n.371+2970G>T
XR_001743495.2:n.543+2970G>T
XR_001743496.2:n.938+2970G>T
XR_001743500.1:n.538+2970G>T
XR_001743501.1:n.538+2970G>T
XR_926265.2:n.538+2970G>T
XR_926266.2:n.651+2970G>T
XR_926267.2:n.538+2970G>T