Canonical Allele Identifier: CA1583149736

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390631T= , CM000667.2:g.132390631T=	GRCh38
NC_000005.9:g.131726323T= , CM000667.1:g.131726323T=	GRCh37
NC_000005.8:g.131754222T=	NCBI36
NG_008982.1:g.25923T=
NG_008982.2:g.25928T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-59T=	ENSP00000388838.2:n.894-59T=
ENST00000435065.7:c.1125-59T=	ENSP00000402760.2:n.1125-59T=
ENST00000448810.6:c.1053-145T=	ENSP00000401860.2:n.1053-145T=
ENST00000685543.1:n.1194-59T=
ENST00000686757.1:c.*217-59T=	ENSP00000510721.1:n.*217-59T=
ENST00000687740.1:n.3738-59T=
ENST00000688151.1:n.2363-59T=
ENST00000689271.1:c.900-59T=	ENSP00000510797.1:n.900-59T=
ENST00000690900.1:c.*217-59T=	ENSP00000510703.1:n.*217-59T=
ENST00000692212.1:n.2606T=
ENST00000692355.1:c.306-59T=
ENST00000692413.1:c.1035-59T=	ENSP00000509374.1:n.1035-59T=
ENST00000692825.1:c.1121-59T=	ENSP00000509447.1:n.1121-59T=
ENST00000693308.1:c.1101-59T=	ENSP00000509770.1:n.1101-59T=
ENST00000693763.1:n.2213-59T=
ENST00000245407.8:c.1053-59T= MANE Select	ENSP00000245407.3:n.1053-59T=
ENST00000245407.7:c.1053-59T=	ENSP00000245407.3:n.1053-59T=
ENST00000435065.6:c.1125-59T=	ENSP00000402760.2:n.1125-59T=
ENST00000447841.5:c.111+1610T=
ENST00000448810.5:c.401-145T=
ENST00000461013.5:n.8475-59T=
ENST00000475308.1:n.1672T=
ENST00000479605.5:n.156-59T=
NM_001308122.1:c.1125-59T=	NP_001295051.1:n.1125-59T=
NM_003060.3:c.1053-59T=	NP_003051.1:n.1053-59T=
XM_011543590.1:c.435-59T=	XP_011541892.1:n.435-59T=
XR_427718.1:n.1413-59T=
XR_948290.1:n.1393+1610T=
XR_948291.1:n.1407-59T=
XM_011543590.2:c.435-59T=	XP_011541892.1:n.435-59T=
XM_017009778.2:c.525-59T=	XP_016865267.1:n.525-59T=
XR_001742215.1:n.1394-145T=
XR_001742216.1:n.1413-145T=
XR_427718.2:n.1413-59T=
XR_948290.2:n.1393+1610T=
XR_948291.2:n.1407-59T=
NM_003060.4:c.1053-59T= MANE Select	NP_003051.1:n.1053-59T=
NM_001308122.2:c.1125-59T=	NP_001295051.1:n.1125-59T=