Canonical Allele Identifier: CA1583149951

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390736A= , CM000667.2:g.132390736A=	GRCh38
NC_000005.9:g.131726428A= , CM000667.1:g.131726428A=	GRCh37
NC_000005.8:g.131754327A=	NCBI36
NG_008982.1:g.26028A=
NG_008982.2:g.26033A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.940A=	ENSP00000388838.2:p.Asn314=
ENST00000435065.7:c.1171A=	ENSP00000402760.2:p.Asn391=
ENST00000448810.6:c.1053-40A=	ENSP00000401860.2:n.1053-40A=
ENST00000685543.1:n.1240A=
ENST00000686757.1:c.*263A=	ENSP00000510721.1:n.*263A=
ENST00000687740.1:n.3784A=
ENST00000688151.1:n.2409A=
ENST00000689271.1:c.946A=	ENSP00000510797.1:p.Asn316=
ENST00000690900.1:c.*263A=	ENSP00000510703.1:n.*263A=
ENST00000692212.1:n.2711A=
ENST00000692355.1:c.352A=
ENST00000692413.1:c.1081A=	ENSP00000509374.1:p.Asn361=
ENST00000692825.1:c.1167A=	ENSP00000509447.1:n.1167A=
ENST00000693308.1:c.1147A=	ENSP00000509770.1:p.Asn383=
ENST00000693763.1:n.2259A=
ENST00000245407.8:c.1099A= MANE Select	ENSP00000245407.3:p.Asn367=
ENST00000245407.7:c.1099A=	ENSP00000245407.3:p.Asn367=
ENST00000435065.6:c.1171A=	ENSP00000402760.2:p.Asn391=
ENST00000447841.5:c.112-1697A=
ENST00000448810.5:c.401-40A=
ENST00000461013.5:n.8521A=
ENST00000475308.1:n.1777A=
ENST00000479605.5:n.202A=
NM_001308122.1:c.1171A=	NP_001295051.1:p.Asn391=
NM_003060.3:c.1099A=	NP_003051.1:p.Asn367=
XM_011543590.1:c.481A=	XP_011541892.1:p.Asn161=
XR_427718.1:n.1459A=
XR_948290.1:n.1394-1697A=
XR_948291.1:n.1453A=
XM_011543590.2:c.481A=	XP_011541892.1:p.Asn161=
XM_017009778.2:c.571A=	XP_016865267.1:p.Asn191=
XR_001742215.1:n.1394-40A=
XR_001742216.1:n.1413-40A=
XR_427718.2:n.1459A=
XR_948290.2:n.1394-1697A=
XR_948291.2:n.1453A=
NM_003060.4:c.1099A= MANE Select	NP_003051.1:p.Asn367=
NM_001308122.2:c.1171A=	NP_001295051.1:p.Asn391=