Canonical Allele Identifier: CA2685364807

Gene: KEL

Linked Data

• gnomAD v4: 7-142958169-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142958169T>C , CM000669.2:g.142958169T>C	GRCh38
NC_000007.13:g.142655256T>C , CM000669.1:g.142655256T>C	GRCh37
NC_000007.12:g.142365378T>C	NCBI36
NG_007492.1:g.9248A>G
NG_007492.2:g.9248A>G
NG_007492.3:g.9248A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.525+135A>G MANE Select	ENSP00000347409.2:n.525+135A>G
ENST00000467543.6:c.*377+135A>G	ENSP00000420011.2:n.*377+135A>G
ENST00000355265.6:c.525+135A>G	ENSP00000347409.2:n.525+135A>G
ENST00000467543.5:c.468+135A>G	ENSP00000420011.1:n.468+135A>G
ENST00000476829.5:c.525+135A>G	ENSP00000419889.1:n.525+135A>G
ENST00000479768.6:n.643+135A>G
ENST00000494148.1:n.124+135A>G
NM_000420.2:c.525+135A>G	NP_000411.1:n.525+135A>G
XM_005249993.2:c.561+135A>G	XP_005250050.1:n.561+135A>G
NM_000420.3:c.525+135A>G MANE Select	NP_000411.1:n.525+135A>G