Canonical Allele Identifier: CA2229715116

Gene: SLC7A6 SLC7A6OS

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68292297A>T , CM000678.2:g.68292297A>T	GRCh38
NC_000016.9:g.68326200A>T , CM000678.1:g.68326200A>T	GRCh37
NC_000016.8:g.66883701A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219343.11:c.1022+636A>T (SLC7A6) MANE Select	ENSP00000219343.6:n.1022+636A>T
ENST00000648130.1:c.*490+636A>T (SLC7A6)	ENSP00000496833.1:n.*490+636A>T
ENST00000219343.10:c.1022+636A>T (SLC7A6)	ENSP00000219343.6:n.1022+636A>T
ENST00000379152.7:c.*187+636A>T (SLC7A6)	ENSP00000368448.3:n.*187+636A>T
ENST00000562863.1:n.376+636A>T (SLC7A6)
ENST00000563208.1:n.475+636A>T (SLC7A6)
ENST00000566454.5:c.1022+636A>T (SLC7A6)	ENSP00000455064.1:n.1022+636A>T
ENST00000567346.5:c.340+636A>T (SLC7A6)	ENSP00000463394.1:n.340+636A>T
ENST00000568315.1:c.236-7602T>A (SLC7A6OS)
ENST00000618043.4:c.*187+636A>T (SLC7A6)	ENSP00000484012.1:n.*187+636A>T
NM_001076785.2:c.1022+636A>T (SLC7A6)	NP_001070253.1:n.1022+636A>T
NM_003983.5:c.1022+636A>T (SLC7A6)	NP_003974.3:n.1022+636A>T
XM_011523433.1:c.1022+636A>T (SLC7A6)	XP_011521735.1:n.1022+636A>T
XM_011523434.1:c.1022+636A>T (SLC7A6)	XP_011521736.1:n.1022+636A>T
XM_011523435.1:c.1022+636A>T (SLC7A6)	XP_011521737.1:n.1022+636A>T
XM_011523436.1:c.1022+636A>T (SLC7A6)	XP_011521738.1:n.1022+636A>T
XM_011523437.1:c.1022+636A>T (SLC7A6)	XP_011521739.1:n.1022+636A>T
XM_011523438.1:c.1022+636A>T (SLC7A6)	XP_011521740.1:n.1022+636A>T
XM_011523439.1:c.398+636A>T (SLC7A6)	XP_011521741.1:n.398+636A>T
XR_243433.2:n.1934+636A>T (SLC7A6)
XM_011523438.2:c.1022+636A>T (SLC7A6)	XP_011521740.1:n.1022+636A>T
XM_024450486.1:c.1022+636A>T (SLC7A6)	XP_024306254.1:n.1022+636A>T
XM_024450487.1:c.1022+636A>T (SLC7A6)	XP_024306255.1:n.1022+636A>T
XM_024450488.1:c.1022+636A>T (SLC7A6)	XP_024306256.1:n.1022+636A>T
XR_001752018.1:n.1301+636A>T (SLC7A6)
XR_001752019.2:n.1352+636A>T (SLC7A6)
XR_001752020.1:n.1414+636A>T (SLC7A6)
XR_002957851.1:n.1447+636A>T (SLC7A6)
XR_243433.3:n.1248+636A>T (SLC7A6)
NM_003983.6:c.1022+636A>T (SLC7A6) MANE Select	NP_003974.3:n.1022+636A>T
NM_001076785.3:c.1022+636A>T (SLC7A6)	NP_001070253.1:n.1022+636A>T