Canonical Allele Identifier: CA2842566964

Gene: KEL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142958035del , CM000669.2:g.142958035del	GRCh38
NC_000007.13:g.142655122del , CM000669.1:g.142655122del	GRCh37
NC_000007.12:g.142365244del	NCBI36
NG_007492.1:g.9383del
NG_007492.2:g.9383del
NG_007492.3:g.9383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.526-61del MANE Select	ENSP00000347409.2:n.526-61del
ENST00000467543.6:c.*378-61del	ENSP00000420011.2:n.*378-61del
ENST00000355265.6:c.526-61del	ENSP00000347409.2:n.526-61del
ENST00000467543.5:c.469-61del	ENSP00000420011.1:n.469-61del
ENST00000476829.5:c.525+270del	ENSP00000419889.1:n.525+270del
ENST00000479768.6:n.644-61del
ENST00000494148.1:n.125-61del
NM_000420.2:c.526-61del	NP_000411.1:n.526-61del
XM_005249993.2:c.562-61del	XP_005250050.1:n.562-61del
NM_000420.3:c.526-61del MANE Select	NP_000411.1:n.526-61del