Canonical Allele Identifier: CA1748724535
Gene: KEL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142957997G= , CM000669.2:g.142957997G= GRCh38
NC_000007.13:g.142655084G= , CM000669.1:g.142655084G= GRCh37
NC_000007.12:g.142365206G= NCBI36
NG_007492.1:g.9420C=
NG_007492.2:g.9420C=
NG_007492.3:g.9420C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355265.7:c.526-24C= MANE Select ENSP00000347409.2:n.526-24C=
ENST00000467543.6:c.*378-24C= ENSP00000420011.2:n.*378-24C=
ENST00000355265.6:c.526-24C= ENSP00000347409.2:n.526-24C=
ENST00000467543.5:c.469-24C= ENSP00000420011.1:n.469-24C=
ENST00000476829.5:c.525+307C= ENSP00000419889.1:n.525+307C=
ENST00000479768.6:n.644-24C=
ENST00000494148.1:n.125-24C=
NM_000420.2:c.526-24C= NP_000411.1:n.526-24C=
XM_005249993.2:c.562-24C= XP_005250050.1:n.562-24C=
NM_000420.3:c.526-24C= MANE Select NP_000411.1:n.526-24C=
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