Canonical Allele Identifier: CA369631032

Gene: KEL

Linked Data

• MyVariant Identifiers: chr7:g.142655001T>A (hg19) ; chr7:g.142957914T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142957914T>A , CM000669.2:g.142957914T>A	GRCh38
NC_000007.13:g.142655001T>A , CM000669.1:g.142655001T>A	GRCh37
NC_000007.12:g.142365123T>A	NCBI36
NG_007492.1:g.9503A>T
NG_007492.2:g.9503A>T
NG_007492.3:g.9503A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.585A>T MANE Select	ENSP00000347409.2:p.Arg195Ser
ENST00000467543.6:c.*437A>T	ENSP00000420011.2:n.*437A>T
ENST00000355265.6:c.585A>T	ENSP00000347409.2:p.Arg195Ser
ENST00000467543.5:c.528A>T	ENSP00000420011.1:p.Arg176Ser
ENST00000476829.5:c.525+390A>T	ENSP00000419889.1:n.525+390A>T
ENST00000479768.6:n.703A>T
ENST00000494148.1:n.184A>T
NM_000420.2:c.585A>T	NP_000411.1:p.Arg195Ser
XM_005249993.2:c.621A>T	XP_005250050.1:p.Arg207Ser
NM_000420.3:c.585A>T MANE Select	NP_000411.1:p.Arg195Ser