Canonical Allele Identifier: CA2685364674
Gene: KEL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142957794G>A , CM000669.2:g.142957794G>A GRCh38
NC_000007.13:g.142654881G>A , CM000669.1:g.142654881G>A GRCh37
NC_000007.12:g.142365003G>A NCBI36
NG_007492.1:g.9623C>T
NG_007492.2:g.9623C>T
NG_007492.3:g.9623C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355265.7:c.672+33C>T MANE Select ENSP00000347409.2:n.672+33C>T
ENST00000355265.6:c.672+33C>T ENSP00000347409.2:n.672+33C>T
ENST00000476829.5:c.525+510C>T ENSP00000419889.1:n.525+510C>T
ENST00000479768.6:n.790+33C>T
ENST00000494148.1:n.271+33C>T
NM_000420.2:c.672+33C>T NP_000411.1:n.672+33C>T
XM_005249993.2:c.708+33C>T XP_005250050.1:n.708+33C>T
NM_000420.3:c.672+33C>T MANE Select NP_000411.1:n.672+33C>T