Canonical Allele Identifier: CA1748724534
Gene: KEL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142957996T= , CM000669.2:g.142957996T= GRCh38
NC_000007.13:g.142655083T= , CM000669.1:g.142655083T= GRCh37
NC_000007.12:g.142365205T= NCBI36
NG_007492.1:g.9421A=
NG_007492.2:g.9421A=
NG_007492.3:g.9421A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355265.7:c.526-23A= MANE Select ENSP00000347409.2:n.526-23A=
ENST00000467543.6:c.*378-23A= ENSP00000420011.2:n.*378-23A=
ENST00000355265.6:c.526-23A= ENSP00000347409.2:n.526-23A=
ENST00000467543.5:c.469-23A= ENSP00000420011.1:n.469-23A=
ENST00000476829.5:c.525+308A= ENSP00000419889.1:n.525+308A=
ENST00000479768.6:n.644-23A=
ENST00000494148.1:n.125-23A=
NM_000420.2:c.526-23A= NP_000411.1:n.526-23A=
XM_005249993.2:c.562-23A= XP_005250050.1:n.562-23A=
NM_000420.3:c.526-23A= MANE Select NP_000411.1:n.526-23A=
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