Canonical Allele Identifier: CA7104684

Gene: SLC7A7

Linked Data

• dbSNP Id: rs762534363
• ExAC: 14:23249298 A / AC
• gnomAD v2: 14-23249298-A-AC
• gnomAD v3: 14-22780089-A-AC
• gnomAD v4: 14-22780089-A-AC
• MyVariant Identifiers: chr14:g.23249298_23249299insC (hg19) ; chr14:g.22780089_22780090insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22780091dup , CM000676.2:g.22780091dup	GRCh38
NC_000014.8:g.23249300dup , CM000676.1:g.23249300dup	GRCh37
NC_000014.7:g.22319140dup	NCBI36
NG_012851.2:g.54731dup , LRG_695:g.54731dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555911.2:c.500-39dup	ENSP00000452551.2:n.500-39dup
ENST00000698939.1:c.500-39dup	ENSP00000514047.1:n.500-39dup
ENST00000397532.9:c.500-39dup	ENSP00000380666.4:n.500-39dup
ENST00000674313.1:c.500-39dup MANE Select	ENSP00000501493.1:n.500-39dup
ENST00000285850.11:c.500-39dup	ENSP00000285850.7:n.500-39dup
ENST00000397528.8:c.500-39dup	ENSP00000380662.4:n.500-39dup
ENST00000397529.6:c.500-39dup	ENSP00000380663.2:n.500-39dup
ENST00000397532.7:c.500-39dup	ENSP00000380666.3:n.500-39dup
ENST00000554061.5:n.171-39dup
ENST00000554517.5:c.-299-39dup	ENSP00000452083.1:n.-299-39dup
ENST00000555702.5:c.500-39dup	ENSP00000451881.1:n.500-39dup
ENST00000556287.5:c.500-39dup	ENSP00000450715.1:n.500-39dup
NM_001126105.2:c.500-39dup , LRG_695t1:c.500-39dup	NP_001119577.1:n.500-39dup
NM_001126106.2:c.500-39dup , LRG_695t2:c.500-39dup	NP_001119578.1:n.500-39dup
NR_040448.1:n.1115-39dup
XM_006720302.1:c.500-39dup	XP_006720365.1:n.500-39dup
XM_011537298.1:c.500-39dup	XP_011535600.1:n.500-39dup
XM_011537299.1:c.500-39dup	XP_011535601.1:n.500-39dup
XM_006720302.2:c.500-39dup	XP_006720365.1:n.500-39dup
XM_011537298.3:c.500-39dup	XP_011535600.1:n.500-39dup
NM_001126105.3:c.500-39dup	NP_001119577.1:n.500-39dup
NM_001126106.4:c.500-39dup	NP_001119578.1:n.500-39dup
NM_003982.4:c.500-39dup MANE Select	NP_003973.3:n.500-39dup