Canonical Allele Identifier: CA834472518

Gene: KEL

Linked Data

• dbSNP Id: rs1257999349
• MyVariant Identifiers: chr7:g.142655166C>T (hg19) ; chr7:g.142958079C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142958079C>T , CM000669.2:g.142958079C>T	GRCh38
NC_000007.13:g.142655166C>T , CM000669.1:g.142655166C>T	GRCh37
NC_000007.12:g.142365288C>T	NCBI36
NG_007492.1:g.9338G>A
NG_007492.2:g.9338G>A
NG_007492.3:g.9338G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.526-106G>A MANE Select	ENSP00000347409.2:n.526-106G>A
ENST00000467543.6:c.*378-106G>A	ENSP00000420011.2:n.*378-106G>A
ENST00000355265.6:c.526-106G>A	ENSP00000347409.2:n.526-106G>A
ENST00000467543.5:c.469-106G>A	ENSP00000420011.1:n.469-106G>A
ENST00000476829.5:c.525+225G>A	ENSP00000419889.1:n.525+225G>A
ENST00000479768.6:n.644-106G>A
ENST00000494148.1:n.125-106G>A
NM_000420.2:c.526-106G>A	NP_000411.1:n.526-106G>A
XM_005249993.2:c.562-106G>A	XP_005250050.1:n.562-106G>A
NM_000420.3:c.526-106G>A MANE Select	NP_000411.1:n.526-106G>A