Canonical Allele Identifier: CA7104814

Gene: SLC7A7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22815939T>C , CM000676.2:g.22815939T>C	GRCh38
NC_000014.8:g.23285148T>C , CM000676.1:g.23285148T>C	GRCh37
NC_000014.7:g.22354988T>C	NCBI36
NG_012851.2:g.18882A>G , LRG_695:g.18882A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698939.1:c.-180-488A>G	ENSP00000514047.1:n.-180-488A>G
ENST00000285850.11:c.-180-488A>G	ENSP00000285850.7:n.-180-488A>G
ENST00000397529.6:c.-42-2499A>G	ENSP00000380663.2:n.-42-2499A>G
ENST00000488800.5:c.-174-488A>G	ENSP00000421554.1:n.-174-488A>G
ENST00000553351.1:n.429-488A>G
ENST00000553632.1:n.347-488A>G
ENST00000553874.5:n.413-488A>G
ENST00000554517.5:c.-300+3699A>G	ENSP00000452083.1:n.-300+3699A>G
ENST00000554741.5:c.-174-488A>G	ENSP00000451063.1:n.-174-488A>G
ENST00000555702.5:c.-174-488A>G	ENSP00000451881.1:n.-174-488A>G
ENST00000556287.5:c.-662A>G	ENSP00000450715.1:n.-662A>G
ENST00000557129.5:c.-175+183A>G	ENSP00000450729.1:n.-175+183A>G
ENST00000557629.5:c.-174-488A>G	ENSP00000450495.1:n.-174-488A>G
NM_001126106.2:c.-174-488A>G , LRG_695t2:c.-174-488A>G	NP_001119578.1:n.-174-488A>G
XM_006720302.1:c.-180-488A>G	XP_006720365.1:n.-180-488A>G
XM_011537299.1:c.-42-2499A>G	XP_011535601.1:n.-42-2499A>G
XM_006720302.2:c.-180-488A>G	XP_006720365.1:n.-180-488A>G
NM_001126106.4:c.-174-488A>G	NP_001119578.1:n.-174-488A>G