Canonical Allele Identifier: CA704246925

Gene: SLC7A7

Linked Data

• dbSNP Id: rs1440353317
• gnomAD v3: 14-22780279-AAAC-A
• gnomAD v4: 14-22780279-AAAC-A
• MyVariant Identifiers: chr14:g.23249489_23249491del (hg19) ; chr14:g.22780280_22780282del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22780282_22780284del , CM000676.2:g.22780282_22780284del	GRCh38
NC_000014.8:g.23249491_23249493del , CM000676.1:g.23249491_23249493del	GRCh37
NC_000014.7:g.22319331_22319333del	NCBI36
NG_012851.2:g.54539_54541del , LRG_695:g.54539_54541del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555911.2:c.500-231_500-229del	ENSP00000452551.2:n.500-231_500-229del
ENST00000698939.1:c.500-231_500-229del	ENSP00000514047.1:n.500-231_500-229del
ENST00000397532.9:c.500-231_500-229del	ENSP00000380666.4:n.500-231_500-229del
ENST00000674313.1:c.500-231_500-229del MANE Select	ENSP00000501493.1:n.500-231_500-229del
ENST00000285850.11:c.500-231_500-229del	ENSP00000285850.7:n.500-231_500-229del
ENST00000397528.8:c.500-231_500-229del	ENSP00000380662.4:n.500-231_500-229del
ENST00000397529.6:c.500-231_500-229del	ENSP00000380663.2:n.500-231_500-229del
ENST00000397532.7:c.500-231_500-229del	ENSP00000380666.3:n.500-231_500-229del
ENST00000554061.5:n.170+24_170+26del
ENST00000554517.5:c.-299-231_-299-229del	ENSP00000452083.1:n.-299-231_-299-229del
ENST00000555702.5:c.500-231_500-229del	ENSP00000451881.1:n.500-231_500-229del
ENST00000556287.5:c.500-231_500-229del	ENSP00000450715.1:n.500-231_500-229del
NM_001126105.2:c.500-231_500-229del , LRG_695t1:c.500-231_500-229del	NP_001119577.1:n.500-231_500-229del
NM_001126106.2:c.500-231_500-229del , LRG_695t2:c.500-231_500-229del	NP_001119578.1:n.500-231_500-229del
NR_040448.1:n.1115-231_1115-229del
XM_006720302.1:c.500-231_500-229del	XP_006720365.1:n.500-231_500-229del
XM_011537298.1:c.500-231_500-229del	XP_011535600.1:n.500-231_500-229del
XM_011537299.1:c.500-231_500-229del	XP_011535601.1:n.500-231_500-229del
XM_006720302.2:c.500-231_500-229del	XP_006720365.1:n.500-231_500-229del
XM_011537298.3:c.500-231_500-229del	XP_011535600.1:n.500-231_500-229del
NM_001126105.3:c.500-231_500-229del	NP_001119577.1:n.500-231_500-229del
NM_001126106.4:c.500-231_500-229del	NP_001119578.1:n.500-231_500-229del
NM_003982.4:c.500-231_500-229del MANE Select	NP_003973.3:n.500-231_500-229del