Canonical Allele Identifier: CA7104324

Gene: SLC7A7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22773338G>A , CM000676.2:g.22773338G>A	GRCh38
NC_000014.8:g.23242547G>A , CM000676.1:g.23242547G>A	GRCh37
NC_000014.7:g.22312387G>A	NCBI36
NG_012851.2:g.61483C>T , LRG_695:g.61483C>T
NG_051068.1:g.11817G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003982.4:c.*272C>T MANE Select	NP_003973.3:n.*272C>T
ENST00000674313.1:c.*272C>T MANE Select	ENSP00000501493.1:n.*272C>T
NM_001126105.2:c.*272C>T , LRG_695t1:c.*272C>T	NP_001119577.1:n.*272C>T
NM_001126105.3:c.*272C>T	NP_001119577.1:n.*272C>T
NM_001126106.2:c.*272C>T , LRG_695t2:c.*272C>T	NP_001119578.1:n.*272C>T
NM_001126106.4:c.*272C>T	NP_001119578.1:n.*272C>T
NR_040448.1:n.2423C>T
ENST00000285850.11:c.*272C>T	ENSP00000285850.7:n.*272C>T
ENST00000397528.8:c.*272C>T	ENSP00000380662.4:n.*272C>T
ENST00000397529.6:c.*272C>T	ENSP00000380663.2:n.*272C>T
ENST00000397532.7:c.*272C>T	ENSP00000380666.3:n.*272C>T
ENST00000397532.9:c.*272C>T	ENSP00000380666.4:n.*272C>T
ENST00000554061.5:n.1479C>T
ENST00000555702.5:c.*272C>T	ENSP00000451881.1:n.*272C>T
ENST00000555911.2:c.*272C>T	ENSP00000452551.2:n.*272C>T
ENST00000556287.5:c.*771C>T	ENSP00000450715.1:n.*771C>T
ENST00000698939.1:c.*874C>T	ENSP00000514047.1:n.*874C>T
XM_006720302.1:c.*272C>T	XP_006720365.1:n.*272C>T
XM_006720302.2:c.*272C>T	XP_006720365.1:n.*272C>T
XM_011537298.1:c.*272C>T	XP_011535600.1:n.*272C>T
XM_011537298.3:c.*272C>T	XP_011535600.1:n.*272C>T
XM_011537299.1:c.*272C>T	XP_011535601.1:n.*272C>T