Canonical Allele Identifier: CA458279127
Gene: KEL HGNC NCBI

Linked Data

dbSNP Id: rs1194784105

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142957887G>A , CM000669.2:g.142957887G>A GRCh38
NC_000007.13:g.142654974G>A , CM000669.1:g.142654974G>A GRCh37
NC_000007.12:g.142365096G>A NCBI36
NG_007492.1:g.9530C>T
NG_007492.2:g.9530C>T
NG_007492.3:g.9530C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355265.7:c.612C>T MANE Select ENSP00000347409.2:p.Phe204=
ENST00000467543.6:c.*464C>T ENSP00000420011.2:n.*464C>T
ENST00000355265.6:c.612C>T ENSP00000347409.2:p.Phe204=
ENST00000467543.5:c.555C>T ENSP00000420011.1:p.Phe185=
ENST00000476829.5:c.525+417C>T ENSP00000419889.1:n.525+417C>T
ENST00000479768.6:n.730C>T
ENST00000494148.1:n.211C>T
NM_000420.2:c.612C>T NP_000411.1:p.Phe204=
XM_005249993.2:c.648C>T XP_005250050.1:p.Phe216=
NM_000420.3:c.612C>T MANE Select NP_000411.1:p.Phe204=