Canonical Allele Identifier: CA253799
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 6208
ClinVar RCV Id: RCV000006586
dbSNP Id: rs121908676

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22813398T>G , CM000676.2:g.22813398T>G GRCh38
NC_000014.8:g.23282607T>G , CM000676.1:g.23282607T>G GRCh37
NC_000014.7:g.22352447T>G NCBI36
NG_012851.2:g.21423A>C , LRG_695:g.21423A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000555911.2:c.1A>C ENSP00000452551.2:p.Met1Leu
ENST00000698939.1:c.1A>C ENSP00000514047.1:p.Met1Leu
ENST00000397532.9:c.1A>C ENSP00000380666.4:p.Met1Leu
ENST00000674313.1:c.1A>C MANE Select ENSP00000501493.1:p.Met1Leu
ENST00000285850.11:c.1A>C ENSP00000285850.7:p.Met1Leu
ENST00000397528.8:c.1A>C ENSP00000380662.4:p.Met1Leu
ENST00000397529.6:c.1A>C ENSP00000380663.2:p.Met1Leu
ENST00000397532.7:c.1A>C ENSP00000380666.3:p.Met1Leu
ENST00000488800.5:c.1A>C ENSP00000421554.1:p.Met1Leu
ENST00000554517.5:c.-300+6240A>C ENSP00000452083.1:n.-300+6240A>C
ENST00000554741.5:c.1A>C ENSP00000451063.1:p.Met1Leu
ENST00000554758.1:c.1A>C ENSP00000450671.1:p.Met1Leu
ENST00000555251.1:c.1A>C ENSP00000451983.1:p.Met1Leu
ENST00000555702.5:c.1A>C ENSP00000451881.1:p.Met1Leu
ENST00000555911.1:c.1A>C ENSP00000452551.1:p.Met1Leu
ENST00000555959.1:c.1A>C ENSP00000452256.1:p.Met1Leu
ENST00000556287.5:c.1A>C ENSP00000450715.1:p.Met1Leu
ENST00000557129.5:c.1A>C ENSP00000450729.1:p.Met1Leu
ENST00000557629.5:c.1A>C ENSP00000450495.1:p.Met1Leu
NM_001126105.2:c.1A>C , LRG_695t1:c.1A>C NP_001119577.1:p.Met1Leu
NM_001126106.2:c.1A>C , LRG_695t2:c.1A>C NP_001119578.1:p.Met1Leu
NR_040448.1:n.616A>C
XM_006720302.1:c.1A>C XP_006720365.1:p.Met1Leu
XM_011537298.1:c.1A>C XP_011535600.1:p.Met1Leu
XM_011537299.1:c.1A>C XP_011535601.1:p.Met1Leu
XM_006720302.2:c.1A>C XP_006720365.1:p.Met1Leu
XM_011537298.3:c.1A>C XP_011535600.1:p.Met1Leu
NM_001126105.3:c.1A>C NP_001119577.1:p.Met1Leu
NM_001126106.4:c.1A>C NP_001119578.1:p.Met1Leu
NM_003982.4:c.1A>C MANE Select NP_003973.3:p.Met1Leu