Canonical Allele Identifier: CA2300488200

Gene: SLC14A2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45682394G= , CM000680.2:g.45682394G=	GRCh38
NC_000018.9:g.43262359G= , CM000680.1:g.43262359G=	GRCh37
NC_000018.8:g.41516357G=	NCBI36
NG_011775.4:g.370G=

Transcript Alleles

HGVS	Amino-acid Change
NM_007163.4:c.2638G= MANE Select	NP_009094.3:p.Ala880=
ENST00000255226.11:c.2638G= MANE Select	ENSP00000255226.5:p.Ala880=
NM_001242692.1:c.2638G=	NP_001229621.1:p.Ala880=
NM_001242692.2:c.2638G=	NP_001229621.1:p.Ala880=
NM_001371319.1:c.2638G=	NP_001358248.1:p.Ala880=
NM_007163.3:c.2638G=	NP_009094.3:p.Ala880=
ENST00000255226.10:c.2638G=	ENSP00000255226.5:p.Ala880=
ENST00000586448.5:c.2638G=	ENSP00000465953.1:p.Ala880=
ENST00000589658.5:c.2638G=	ENSP00000465349.2:p.Ala880=
XM_011526216.1:c.2638G=	XP_011524518.1:p.Ala880=
XM_011526217.1:c.2503G=	XP_011524519.1:p.Ala835=
XM_017026016.2:c.2503G=	XP_016881505.1:p.Ala835=
XM_024451270.1:c.2638G=	XP_024307038.1:p.Ala880=
XM_024451271.1:c.2638G=	XP_024307039.1:p.Ala880=
XR_935423.2:n.872+10001C=