Canonical Allele Identifier: CA1748724559

Gene: KEL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142958043C= , CM000669.2:g.142958043C=	GRCh38
NC_000007.13:g.142655130C= , CM000669.1:g.142655130C=	GRCh37
NC_000007.12:g.142365252C=	NCBI36
NG_007492.1:g.9374G=
NG_007492.2:g.9374G=
NG_007492.3:g.9374G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.526-70G= MANE Select	ENSP00000347409.2:n.526-70G=
ENST00000467543.6:c.*378-70G=	ENSP00000420011.2:n.*378-70G=
ENST00000355265.6:c.526-70G=	ENSP00000347409.2:n.526-70G=
ENST00000467543.5:c.469-70G=	ENSP00000420011.1:n.469-70G=
ENST00000476829.5:c.525+261G=	ENSP00000419889.1:n.525+261G=
ENST00000479768.6:n.644-70G=
ENST00000494148.1:n.125-70G=
NM_000420.2:c.526-70G=	NP_000411.1:n.526-70G=
XM_005249993.2:c.562-70G=	XP_005250050.1:n.562-70G=
NM_000420.3:c.526-70G= MANE Select	NP_000411.1:n.526-70G=