Canonical Allele Identifier: CA2300461070

Gene: SLC14A2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45622439C= , CM000680.2:g.45622439C=	GRCh38
NC_000018.9:g.43202404C= , CM000680.1:g.43202404C=	GRCh37
NC_000018.8:g.41456402C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_007163.4:c.-34-2192C= MANE Select	NP_009094.3:n.-34-2192C=
ENST00000255226.11:c.-34-2192C= MANE Select	ENSP00000255226.5:n.-34-2192C=
NM_001242692.1:c.-34-2192C=	NP_001229621.1:n.-34-2192C=
NM_001242692.2:c.-34-2192C=	NP_001229621.1:n.-34-2192C=
NM_001371319.1:c.-34-2192C=	NP_001358248.1:n.-34-2192C=
NM_007163.3:c.-34-2192C=	NP_009094.3:n.-34-2192C=
ENST00000255226.10:c.-34-2192C=	ENSP00000255226.5:n.-34-2192C=
ENST00000323329.3:c.-34-2192C=	ENSP00000320689.3:n.-34-2192C=
ENST00000586448.5:c.-34-2192C=	ENSP00000465953.1:n.-34-2192C=
ENST00000589658.5:c.-34-2192C=	ENSP00000465349.2:n.-34-2192C=
XM_011526216.1:c.-34-2192C=	XP_011524518.1:n.-34-2192C=
XM_011526217.1:c.-34-2192C=	XP_011524519.1:n.-34-2192C=
XM_017026016.2:c.-34-2192C=	XP_016881505.1:n.-34-2192C=
XM_024451270.1:c.-34-2192C=	XP_024307038.1:n.-34-2192C=
XM_024451271.1:c.-34-2192C=	XP_024307039.1:n.-34-2192C=