Canonical Allele Identifier: CA2332455380

Gene: SLC7A9

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32862057G= , CM000681.2:g.32862057G=	GRCh38
NC_000019.9:g.33352963G= , CM000681.1:g.33352963G=	GRCh37
NC_000019.8:g.38044803G=	NCBI36
NG_008258.1:g.12721C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000023064.9:c.704+61C= MANE Select	ENSP00000023064.3:n.704+61C=
ENST00000023064.8:c.704+61C=	ENSP00000023064.3:n.704+61C=
ENST00000587772.1:c.704+61C=	ENSP00000468439.1:n.704+61C=
ENST00000589659.1:n.649+61C=
ENST00000590341.5:c.704+61C=	ENSP00000464822.1:n.704+61C=
ENST00000590465.5:c.*211-1407C=	ENSP00000468076.1:n.*211-1407C=
ENST00000592232.5:c.*211-1407C=	ENSP00000465563.1:n.*211-1407C=
NM_001126335.1:c.704+61C=	NP_001119807.1:n.704+61C=
NM_001243036.1:c.704+61C=	NP_001229965.1:n.704+61C=
NM_014270.4:c.704+61C=	NP_055085.1:n.704+61C=
XM_006722992.1:c.24-1407C=	XP_006723055.1:n.24-1407C=
XM_011526402.1:c.704+61C=	XP_011524704.1:n.704+61C=
XM_011526402.3:c.704+61C=	XP_011524704.1:n.704+61C=
XM_017026230.1:c.440+61C=	XP_016881719.1:n.440+61C=
XM_024451334.1:c.-564-1407C=	XP_024307102.1:n.-564-1407C=
NM_014270.5:c.704+61C= MANE Select	NP_055085.1:n.704+61C=
NM_001126335.2:c.704+61C=	NP_001119807.1:n.704+61C=
NM_001243036.2:c.704+61C=	NP_001229965.1:n.704+61C=