Canonical Allele Identifier: CA13974337
Gene: SLC7A7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22813541A>C , CM000676.2:g.22813541A>C GRCh38
NC_000014.8:g.23282750A>C , CM000676.1:g.23282750A>C GRCh37
NC_000014.7:g.22352590A>C NCBI36
NG_012851.2:g.21280T>G , LRG_695:g.21280T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000555911.2:c.-42-101T>G ENSP00000452551.2:n.-42-101T>G
ENST00000698939.1:c.-42-101T>G ENSP00000514047.1:n.-42-101T>G
ENST00000397532.9:c.-42-101T>G ENSP00000380666.4:n.-42-101T>G
ENST00000674313.1:c.-42-101T>G MANE Select ENSP00000501493.1:n.-42-101T>G
ENST00000285850.11:c.-42-101T>G ENSP00000285850.7:n.-42-101T>G
ENST00000397528.8:c.-42-101T>G ENSP00000380662.4:n.-42-101T>G
ENST00000397529.6:c.-42-101T>G ENSP00000380663.2:n.-42-101T>G
ENST00000397532.7:c.-42-101T>G ENSP00000380666.3:n.-42-101T>G
ENST00000488800.5:c.-42-101T>G ENSP00000421554.1:n.-42-101T>G
ENST00000553351.1:n.561-101T>G
ENST00000553874.5:n.545-101T>G
ENST00000554517.5:c.-300+6097T>G ENSP00000452083.1:n.-300+6097T>G
ENST00000554741.5:c.-42-101T>G ENSP00000451063.1:n.-42-101T>G
ENST00000554758.1:c.-42-101T>G ENSP00000450671.1:n.-42-101T>G
ENST00000555251.1:c.-42-101T>G ENSP00000451983.1:n.-42-101T>G
ENST00000555702.5:c.-42-101T>G ENSP00000451881.1:n.-42-101T>G
ENST00000555911.1:c.-42-101T>G ENSP00000452551.1:n.-42-101T>G
ENST00000555959.1:c.-42-101T>G ENSP00000452256.1:n.-42-101T>G
ENST00000556287.5:c.-42-101T>G ENSP00000450715.1:n.-42-101T>G
ENST00000557129.5:c.-42-101T>G ENSP00000450729.1:n.-42-101T>G
ENST00000557629.5:c.-42-101T>G ENSP00000450495.1:n.-42-101T>G
NM_001126105.2:c.-42-101T>G , LRG_695t1:c.-42-101T>G NP_001119577.1:n.-42-101T>G
NM_001126106.2:c.-42-101T>G , LRG_695t2:c.-42-101T>G NP_001119578.1:n.-42-101T>G
NR_040448.1:n.574-101T>G
XM_006720302.1:c.-42-101T>G XP_006720365.1:n.-42-101T>G
XM_011537298.1:c.-42-101T>G XP_011535600.1:n.-42-101T>G
XM_011537299.1:c.-42-101T>G XP_011535601.1:n.-42-101T>G
XM_006720302.2:c.-42-101T>G XP_006720365.1:n.-42-101T>G
XM_011537298.3:c.-42-101T>G XP_011535600.1:n.-42-101T>G
NM_001126105.3:c.-42-101T>G NP_001119577.1:n.-42-101T>G
NM_001126106.4:c.-42-101T>G NP_001119578.1:n.-42-101T>G
NM_003982.4:c.-42-101T>G MANE Select NP_003973.3:n.-42-101T>G