Canonical Allele Identifier: CA1583149793

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390683G= , CM000667.2:g.132390683G=	GRCh38
NC_000005.9:g.131726375G= , CM000667.1:g.131726375G=	GRCh37
NC_000005.8:g.131754274G=	NCBI36
NG_008982.1:g.25975G=
NG_008982.2:g.25980G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-7G=	ENSP00000388838.2:n.894-7G=
ENST00000435065.7:c.1125-7G=	ENSP00000402760.2:n.1125-7G=
ENST00000448810.6:c.1053-93G=	ENSP00000401860.2:n.1053-93G=
ENST00000685543.1:n.1194-7G=
ENST00000686757.1:c.*217-7G=	ENSP00000510721.1:n.*217-7G=
ENST00000687740.1:n.3738-7G=
ENST00000688151.1:n.2363-7G=
ENST00000689271.1:c.900-7G=	ENSP00000510797.1:n.900-7G=
ENST00000690900.1:c.*217-7G=	ENSP00000510703.1:n.*217-7G=
ENST00000692212.1:n.2658G=
ENST00000692355.1:c.306-7G=
ENST00000692413.1:c.1035-7G=	ENSP00000509374.1:n.1035-7G=
ENST00000692825.1:c.1121-7G=	ENSP00000509447.1:n.1121-7G=
ENST00000693308.1:c.1101-7G=	ENSP00000509770.1:n.1101-7G=
ENST00000693763.1:n.2213-7G=
ENST00000245407.8:c.1053-7G= MANE Select	ENSP00000245407.3:n.1053-7G=
ENST00000245407.7:c.1053-7G=	ENSP00000245407.3:n.1053-7G=
ENST00000435065.6:c.1125-7G=	ENSP00000402760.2:n.1125-7G=
ENST00000447841.5:c.111+1662G=
ENST00000448810.5:c.401-93G=
ENST00000461013.5:n.8475-7G=
ENST00000475308.1:n.1724G=
ENST00000479605.5:n.156-7G=
NM_001308122.1:c.1125-7G=	NP_001295051.1:n.1125-7G=
NM_003060.3:c.1053-7G=	NP_003051.1:n.1053-7G=
XM_011543590.1:c.435-7G=	XP_011541892.1:n.435-7G=
XR_427718.1:n.1413-7G=
XR_948290.1:n.1393+1662G=
XR_948291.1:n.1407-7G=
XM_011543590.2:c.435-7G=	XP_011541892.1:n.435-7G=
XM_017009778.2:c.525-7G=	XP_016865267.1:n.525-7G=
XR_001742215.1:n.1394-93G=
XR_001742216.1:n.1413-93G=
XR_427718.2:n.1413-7G=
XR_948290.2:n.1393+1662G=
XR_948291.2:n.1407-7G=
NM_003060.4:c.1053-7G= MANE Select	NP_003051.1:n.1053-7G=
NM_001308122.2:c.1125-7G=	NP_001295051.1:n.1125-7G=