Canonical Allele Identifier: CA1748724446
Gene: KEL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142957792A= , CM000669.2:g.142957792A= GRCh38
NC_000007.13:g.142654879A= , CM000669.1:g.142654879A= GRCh37
NC_000007.12:g.142365001A= NCBI36
NG_007492.1:g.9625T=
NG_007492.2:g.9625T=
NG_007492.3:g.9625T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355265.7:c.672+35T= MANE Select ENSP00000347409.2:n.672+35T=
ENST00000355265.6:c.672+35T= ENSP00000347409.2:n.672+35T=
ENST00000476829.5:c.525+512T= ENSP00000419889.1:n.525+512T=
ENST00000479768.6:n.790+35T=
ENST00000494148.1:n.271+35T=
NM_000420.2:c.672+35T= NP_000411.1:n.672+35T=
XM_005249993.2:c.708+35T= XP_005250050.1:n.708+35T=
NM_000420.3:c.672+35T= MANE Select NP_000411.1:n.672+35T=
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