Canonical Allele Identifier: CA1748724589

Gene: KEL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142958136T= , CM000669.2:g.142958136T=	GRCh38
NC_000007.13:g.142655223T= , CM000669.1:g.142655223T=	GRCh37
NC_000007.12:g.142365345T=	NCBI36
NG_007492.1:g.9281A=
NG_007492.2:g.9281A=
NG_007492.3:g.9281A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.526-163A= MANE Select	ENSP00000347409.2:n.526-163A=
ENST00000467543.6:c.*378-163A=	ENSP00000420011.2:n.*378-163A=
ENST00000355265.6:c.526-163A=	ENSP00000347409.2:n.526-163A=
ENST00000467543.5:c.469-163A=	ENSP00000420011.1:n.469-163A=
ENST00000476829.5:c.525+168A=	ENSP00000419889.1:n.525+168A=
ENST00000479768.6:n.644-163A=
ENST00000494148.1:n.125-163A=
NM_000420.2:c.526-163A=	NP_000411.1:n.526-163A=
XM_005249993.2:c.562-163A=	XP_005250050.1:n.562-163A=
NM_000420.3:c.526-163A= MANE Select	NP_000411.1:n.526-163A=