Canonical Allele Identifier: CA388923859

Gene: SLC7A7

Linked Data

• MyVariant Identifiers: chr14:g.23245528C>A (hg19) ; chr14:g.22776319C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22776319C>A , CM000676.2:g.22776319C>A	GRCh38
NC_000014.8:g.23245528C>A , CM000676.1:g.23245528C>A	GRCh37
NC_000014.7:g.22315368C>A	NCBI36
NG_012851.2:g.58502G>T , LRG_695:g.58502G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000555911.2:c.771-1G>T	ENSP00000452551.2:n.771-1G>T
ENST00000698939.1:c.771-383G>T	ENSP00000514047.1:n.771-383G>T
ENST00000397532.9:c.771-1G>T	ENSP00000380666.4:n.771-1G>T
ENST00000674313.1:c.771-1G>T MANE Select	ENSP00000501493.1:n.771-1G>T
ENST00000285850.11:c.771-1G>T	ENSP00000285850.7:n.771-1G>T
ENST00000397528.8:c.771-1G>T	ENSP00000380662.4:n.771-1G>T
ENST00000397529.6:c.771-1G>T	ENSP00000380663.2:n.771-1G>T
ENST00000397532.7:c.771-1G>T	ENSP00000380666.3:n.771-1G>T
ENST00000554061.5:n.442-1G>T
ENST00000554517.5:c.-28-1G>T	ENSP00000452083.1:n.-28-1G>T
ENST00000555702.5:c.771-1G>T	ENSP00000451881.1:n.771-1G>T
ENST00000556287.5:c.771-1G>T	ENSP00000450715.1:n.771-1G>T
NM_001126105.2:c.771-1G>T , LRG_695t1:c.771-1G>T	NP_001119577.1:n.771-1G>T
NM_001126106.2:c.771-1G>T , LRG_695t2:c.771-1G>T	NP_001119578.1:n.771-1G>T
NR_040448.1:n.1386-1G>T
XM_006720302.1:c.771-1G>T	XP_006720365.1:n.771-1G>T
XM_011537298.1:c.771-1G>T	XP_011535600.1:n.771-1G>T
XM_011537299.1:c.771-1G>T	XP_011535601.1:n.771-1G>T
XM_006720302.2:c.771-1G>T	XP_006720365.1:n.771-1G>T
XM_011537298.3:c.771-1G>T	XP_011535600.1:n.771-1G>T
NM_001126105.3:c.771-1G>T	NP_001119577.1:n.771-1G>T
NM_001126106.4:c.771-1G>T	NP_001119578.1:n.771-1G>T
NM_003982.4:c.771-1G>T MANE Select	NP_003973.3:n.771-1G>T