Canonical Allele Identifier: CA2579049290
Gene: KEL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142958060G>A , CM000669.2:g.142958060G>A GRCh38
NC_000007.13:g.142655147G>A , CM000669.1:g.142655147G>A GRCh37
NC_000007.12:g.142365269G>A NCBI36
NG_007492.1:g.9357C>T
NG_007492.2:g.9357C>T
NG_007492.3:g.9357C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355265.7:c.526-87C>T MANE Select ENSP00000347409.2:n.526-87C>T
ENST00000467543.6:c.*378-87C>T ENSP00000420011.2:n.*378-87C>T
ENST00000355265.6:c.526-87C>T ENSP00000347409.2:n.526-87C>T
ENST00000467543.5:c.469-87C>T ENSP00000420011.1:n.469-87C>T
ENST00000476829.5:c.525+244C>T ENSP00000419889.1:n.525+244C>T
ENST00000479768.6:n.644-87C>T
ENST00000494148.1:n.125-87C>T
NM_000420.2:c.526-87C>T NP_000411.1:n.526-87C>T
XM_005249993.2:c.562-87C>T XP_005250050.1:n.562-87C>T
NM_000420.3:c.526-87C>T MANE Select NP_000411.1:n.526-87C>T