Canonical Allele Identifier: CA15310025

Gene: KIAA1211

Linked Data

• dbSNP Id: rs629242
• gnomAD: 4:57143037 C / T
• MyVariant Identifiers: chr4:g.57143037C>T (hg19) ; chr4:g.56276871C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.56276871C>T , CM000666.2:g.56276871C>T	GRCh38
NC_000004.11:g.57143037C>T , CM000666.1:g.57143037C>T	GRCh37
NC_000004.10:g.56837794C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264229.10:c.-17+4379C>T	ENSP00000264229.6:p.=
ENST00000504228.5:c.-17+4379C>T	ENSP00000423366.1:p.=
ENST00000541073.5:c.-60+4379C>T	ENSP00000444006.1:p.=
ENST00000629263.2:c.-174+4379C>T	ENSP00000486652.1:p.=
NM_020722.1:c.-17+4379C>T	NP_065773.1:p.=
XM_005265752.2:c.-17+4379C>T	XP_005265809.1:p.=
XM_011534397.1:c.-17+4379C>T	XP_011532699.1:p.=
XM_011534398.1:c.-39+4379C>T	XP_011532700.1:p.=
XM_011534399.1:c.-55+4379C>T	XP_011532701.1:p.=
XM_011534397.3:c.-17+4379C>T	XP_011532699.1:p.=
XM_017008473.1:c.-39+4379C>T	XP_016863962.1:p.=
XM_017008474.1:c.-55+4379C>T	XP_016863963.1:p.=
XM_024454158.1:c.-17+4379C>T	XP_024309926.1:p.=
XM_024454159.1:c.-17+4379C>T	XP_024309927.1:p.=