Canonical Allele Identifier: CA3082085

Gene: SLC7A11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.138219347T>C , CM000666.2:g.138219347T>C	GRCh38
NC_000004.11:g.139140501T>C , CM000666.1:g.139140501T>C	GRCh37
NC_000004.10:g.139359951T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280612.9:c.665A>G MANE Select	ENSP00000280612.5:p.Lys222Arg
ENST00000509248.1:c.65A>G	ENSP00000424046.1:p.Lys22Arg
NM_014331.3:c.665A>G	NP_055146.1:p.Lys222Arg
XM_011531800.1:c.707A>G	XP_011530102.1:p.Lys236Arg
XM_011531801.1:c.707A>G	XP_011530103.1:p.Lys236Arg
XM_011531802.1:c.665A>G	XP_011530104.1:p.Lys222Arg
XM_011531803.1:c.707A>G	XP_011530105.1:p.Lys236Arg
XM_011531804.1:c.707A>G	XP_011530106.1:p.Lys236Arg
XM_011531805.1:c.707A>G	XP_011530107.1:p.Lys236Arg
XM_011531802.3:c.665A>G	XP_011530104.1:p.Lys222Arg
XR_001741190.2:n.945A>G
XR_001741191.2:n.945A>G
NM_014331.4:c.665A>G MANE Select	NP_055146.1:p.Lys222Arg