Canonical Allele Identifier: CA1583141244

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132378230G= , CM000667.2:g.132378230G=	GRCh38
NC_000005.9:g.131713922G= , CM000667.1:g.131713922G=	GRCh37
NC_000005.8:g.131741821G=	NCBI36
NG_008982.1:g.13522G=
NG_008982.2:g.13527G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.394-148G=	ENSP00000388838.2:n.394-148G=
ENST00000435065.7:c.460G=	ENSP00000402760.2:p.Ala154=
ENST00000448810.6:c.394-148G=	ENSP00000401860.2:n.394-148G=
ENST00000686757.1:c.394-148G=	ENSP00000510721.1:n.394-148G=
ENST00000687740.1:n.528-148G=
ENST00000689271.1:c.394-148G=	ENSP00000510797.1:n.394-148G=
ENST00000690900.1:c.394-148G=	ENSP00000510703.1:n.394-148G=
ENST00000692413.1:c.394-148G=	ENSP00000509374.1:n.394-148G=
ENST00000692825.1:c.456G=	ENSP00000509447.1:n.456G=
ENST00000693308.1:c.394-148G=	ENSP00000509770.1:n.394-148G=
ENST00000693763.1:n.528-148G=
ENST00000245407.8:c.394-148G= MANE Select	ENSP00000245407.3:n.394-148G=
ENST00000245407.7:c.394-148G=	ENSP00000245407.3:n.394-148G=
ENST00000415928.5:c.157G=	ENSP00000388838.1:p.Ala53=
ENST00000435065.6:c.460G=	ENSP00000402760.2:p.Ala154=
ENST00000437841.6:c.394-7098G=	ENSP00000400553.1:n.394-7098G=
ENST00000461013.5:n.2145G=
NM_001308122.1:c.460G=	NP_001295051.1:p.Ala154=
NM_003060.3:c.394-148G=	NP_003051.1:n.394-148G=
XR_427718.1:n.729G=
XR_948290.1:n.729G=
XR_948291.1:n.729G=
XM_011543590.2:c.-238-148G=	XP_011541892.1:n.-238-148G=
XM_017009778.2:c.-31-5917G=	XP_016865267.1:n.-31-5917G=
XR_001742215.1:n.729G=
XR_001742216.1:n.729G=
XR_427718.2:n.729G=
XR_948290.2:n.729G=
XR_948291.2:n.729G=
NM_003060.4:c.394-148G= MANE Select	NP_003051.1:n.394-148G=
NM_001308122.2:c.460G=	NP_001295051.1:p.Ala154=