Canonical Allele Identifier: CA1583146028

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132386976T= , CM000667.2:g.132386976T=	GRCh38
NC_000005.9:g.131722668T= , CM000667.1:g.131722668T=	GRCh37
NC_000005.8:g.131750567T=	NCBI36
NG_008982.1:g.22268T=
NG_008982.2:g.22273T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.666-49T=	ENSP00000388838.2:n.666-49T=
ENST00000435065.7:c.897-49T=	ENSP00000402760.2:n.897-49T=
ENST00000448810.6:c.825-49T=	ENSP00000401860.2:n.825-49T=
ENST00000686757.1:c.844-49T=	ENSP00000510721.1:n.844-49T=
ENST00000687740.1:n.3461T=
ENST00000688151.1:n.2135-49T=
ENST00000689271.1:c.672-49T=	ENSP00000510797.1:n.672-49T=
ENST00000690900.1:c.796-49T=	ENSP00000510703.1:n.796-49T=
ENST00000692212.1:n.769-49T=
ENST00000692355.1:c.205-1945T=
ENST00000692413.1:c.844-86T=	ENSP00000509374.1:n.844-86T=
ENST00000692825.1:c.893-49T=	ENSP00000509447.1:n.893-49T=
ENST00000693308.1:c.838-14T=	ENSP00000509770.1:n.838-14T=
ENST00000693763.1:n.1985-49T=
ENST00000245407.8:c.825-49T= MANE Select	ENSP00000245407.3:n.825-49T=
ENST00000245407.7:c.825-49T=	ENSP00000245407.3:n.825-49T=
ENST00000415928.5:c.594-49T=	ENSP00000388838.1:n.594-49T=
ENST00000435065.6:c.897-49T=	ENSP00000402760.2:n.897-49T=
ENST00000437841.6:c.*140-49T=	ENSP00000400553.1:n.*140-49T=
ENST00000448810.5:c.173-49T=
ENST00000461013.5:n.8247-49T=
NM_001308122.1:c.897-49T=	NP_001295051.1:n.897-49T=
NM_003060.3:c.825-49T=	NP_003051.1:n.825-49T=
XM_011543590.1:c.207-49T=	XP_011541892.1:n.207-49T=
XR_427718.1:n.1185-49T=
XR_948290.1:n.1166-49T=
XR_948291.1:n.1179-49T=
XM_011543590.2:c.207-49T=	XP_011541892.1:n.207-49T=
XM_017009778.2:c.297-49T=	XP_016865267.1:n.297-49T=
XR_001742215.1:n.1166-49T=
XR_001742216.1:n.1185-49T=
XR_427718.2:n.1185-49T=
XR_948290.2:n.1166-49T=
XR_948291.2:n.1179-49T=
NM_003060.4:c.825-49T= MANE Select	NP_003051.1:n.825-49T=
NM_001308122.2:c.897-49T=	NP_001295051.1:n.897-49T=