Canonical Allele Identifier: CA1748722859
Gene: KEL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142954181C= , CM000669.2:g.142954181C= GRCh38
NC_000007.13:g.142651268C= , CM000669.1:g.142651268C= GRCh37
NC_000007.12:g.142361390C= NCBI36
NG_007492.1:g.13236G=
NG_007492.2:g.13236G=
NG_007492.3:g.13236G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355265.7:c.924+3G= MANE Select ENSP00000347409.2:n.924+3G=
ENST00000355265.6:c.924+3G= ENSP00000347409.2:n.924+3G=
ENST00000479768.6:n.1042+3G=
NM_000420.2:c.924+3G= NP_000411.1:n.924+3G=
XM_005249993.2:c.960+3G= XP_005250050.1:n.960+3G=
XM_005249994.3:c.-24+3G= XP_005250051.1:n.-24+3G=
NM_000420.3:c.924+3G= MANE Select NP_000411.1:n.924+3G=
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