Canonical Allele Identifier: CA1583149941

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390730A= , CM000667.2:g.132390730A=	GRCh38
NC_000005.9:g.131726422A= , CM000667.1:g.131726422A=	GRCh37
NC_000005.8:g.131754321A=	NCBI36
NG_008982.1:g.26022A=
NG_008982.2:g.26027A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.934A=	ENSP00000388838.2:p.Thr312=
ENST00000435065.7:c.1165A=	ENSP00000402760.2:p.Thr389=
ENST00000448810.6:c.1053-46A=	ENSP00000401860.2:n.1053-46A=
ENST00000685543.1:n.1234A=
ENST00000686757.1:c.*257A=	ENSP00000510721.1:n.*257A=
ENST00000687740.1:n.3778A=
ENST00000688151.1:n.2403A=
ENST00000689271.1:c.940A=	ENSP00000510797.1:p.Thr314=
ENST00000690900.1:c.*257A=	ENSP00000510703.1:n.*257A=
ENST00000692212.1:n.2705A=
ENST00000692355.1:c.346A=
ENST00000692413.1:c.1075A=	ENSP00000509374.1:p.Thr359=
ENST00000692825.1:c.1161A=	ENSP00000509447.1:n.1161A=
ENST00000693308.1:c.1141A=	ENSP00000509770.1:p.Thr381=
ENST00000693763.1:n.2253A=
ENST00000245407.8:c.1093A= MANE Select	ENSP00000245407.3:p.Thr365=
ENST00000245407.7:c.1093A=	ENSP00000245407.3:p.Thr365=
ENST00000435065.6:c.1165A=	ENSP00000402760.2:p.Thr389=
ENST00000447841.5:c.112-1703A=
ENST00000448810.5:c.401-46A=
ENST00000461013.5:n.8515A=
ENST00000475308.1:n.1771A=
ENST00000479605.5:n.196A=
NM_001308122.1:c.1165A=	NP_001295051.1:p.Thr389=
NM_003060.3:c.1093A=	NP_003051.1:p.Thr365=
XM_011543590.1:c.475A=	XP_011541892.1:p.Thr159=
XR_427718.1:n.1453A=
XR_948290.1:n.1394-1703A=
XR_948291.1:n.1447A=
XM_011543590.2:c.475A=	XP_011541892.1:p.Thr159=
XM_017009778.2:c.565A=	XP_016865267.1:p.Thr189=
XR_001742215.1:n.1394-46A=
XR_001742216.1:n.1413-46A=
XR_427718.2:n.1453A=
XR_948290.2:n.1394-1703A=
XR_948291.2:n.1447A=
NM_003060.4:c.1093A= MANE Select	NP_003051.1:p.Thr365=
NM_001308122.2:c.1165A=	NP_001295051.1:p.Thr389=