Canonical Allele Identifier: CA257714475
Gene: SLC7A7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22812655_22812657del , CM000676.2:g.22812655_22812657del GRCh38
NC_000014.8:g.23281864_23281866del , CM000676.1:g.23281864_23281866del GRCh37
NC_000014.7:g.22351704_22351706del NCBI36
NG_012851.2:g.22179_22181del , LRG_695:g.22179_22181del

Transcript Alleles

HGVS Amino-acid Change
ENST00000555911.2:c.499+258_499+260del ENSP00000452551.2:n.499+258_499+260del
ENST00000698939.1:c.499+258_499+260del ENSP00000514047.1:n.499+258_499+260del
ENST00000397532.9:c.499+258_499+260del ENSP00000380666.4:n.499+258_499+260del
ENST00000674313.1:c.499+258_499+260del MANE Select ENSP00000501493.1:n.499+258_499+260del
ENST00000285850.11:c.499+258_499+260del ENSP00000285850.7:n.499+258_499+260del
ENST00000397528.8:c.499+258_499+260del ENSP00000380662.4:n.499+258_499+260del
ENST00000397529.6:c.499+258_499+260del ENSP00000380663.2:n.499+258_499+260del
ENST00000397532.7:c.499+258_499+260del ENSP00000380666.3:n.499+258_499+260del
ENST00000554517.5:c.-300+6996_-300+6998del ENSP00000452083.1:n.-300+6996_-300+6998del
ENST00000555702.5:c.499+258_499+260del ENSP00000451881.1:n.499+258_499+260del
ENST00000556287.5:c.499+258_499+260del ENSP00000450715.1:n.499+258_499+260del
NM_001126105.2:c.499+258_499+260del , LRG_695t1:c.499+258_499+260del NP_001119577.1:n.499+258_499+260del
NM_001126106.2:c.499+258_499+260del , LRG_695t2:c.499+258_499+260del NP_001119578.1:n.499+258_499+260del
NR_040448.1:n.1114+258_1114+260del
XM_006720302.1:c.499+258_499+260del XP_006720365.1:n.499+258_499+260del
XM_011537298.1:c.499+258_499+260del XP_011535600.1:n.499+258_499+260del
XM_011537299.1:c.499+258_499+260del XP_011535601.1:n.499+258_499+260del
XM_006720302.2:c.499+258_499+260del XP_006720365.1:n.499+258_499+260del
XM_011537298.3:c.499+258_499+260del XP_011535600.1:n.499+258_499+260del
NM_001126105.3:c.499+258_499+260del NP_001119577.1:n.499+258_499+260del
NM_001126106.4:c.499+258_499+260del NP_001119578.1:n.499+258_499+260del
NM_003982.4:c.499+258_499+260del MANE Select NP_003973.3:n.499+258_499+260del