Canonical Allele Identifier: CA369631381

Gene: KEL

Linked Data

• MyVariant Identifiers: chr7:g.142655048G>T (hg19) ; chr7:g.142957961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142957961G>T , CM000669.2:g.142957961G>T	GRCh38
NC_000007.13:g.142655048G>T , CM000669.1:g.142655048G>T	GRCh37
NC_000007.12:g.142365170G>T	NCBI36
NG_007492.1:g.9456C>A
NG_007492.2:g.9456C>A
NG_007492.3:g.9456C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.538C>A MANE Select	ENSP00000347409.2:p.Arg180Ser
ENST00000467543.6:c.*390C>A	ENSP00000420011.2:n.*390C>A
ENST00000355265.6:c.538C>A	ENSP00000347409.2:p.Arg180Ser
ENST00000467543.5:c.481C>A	ENSP00000420011.1:p.Arg161Ser
ENST00000476829.5:c.525+343C>A	ENSP00000419889.1:n.525+343C>A
ENST00000479768.6:n.656C>A
ENST00000494148.1:n.137C>A
NM_000420.2:c.538C>A	NP_000411.1:p.Arg180Ser
XM_005249993.2:c.574C>A	XP_005250050.1:p.Arg192Ser
NM_000420.3:c.538C>A MANE Select	NP_000411.1:p.Arg180Ser