Canonical Allele Identifier: CA1583150300

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390896T= , CM000667.2:g.132390896T=	GRCh38
NC_000005.9:g.131726588T= , CM000667.1:g.131726588T=	GRCh37
NC_000005.8:g.131754487T=	NCBI36
NG_008982.1:g.26188T=
NG_008982.2:g.26193T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1100T=	ENSP00000388838.2:p.Val367=
ENST00000435065.7:c.1331T=	ENSP00000402760.2:p.Val444=
ENST00000448810.6:c.*111T=	ENSP00000401860.2:n.*111T=
ENST00000685543.1:n.1400T=
ENST00000686757.1:c.*423T=	ENSP00000510721.1:n.*423T=
ENST00000687740.1:n.3944T=
ENST00000688151.1:n.2569T=
ENST00000689271.1:c.1106T=	ENSP00000510797.1:p.Val369=
ENST00000690900.1:c.*423T=	ENSP00000510703.1:n.*423T=
ENST00000692212.1:n.2871T=
ENST00000692355.1:c.512T=
ENST00000692413.1:c.1241T=	ENSP00000509374.1:p.Val414=
ENST00000692825.1:c.1327T=	ENSP00000509447.1:n.1327T=
ENST00000693308.1:c.1307T=	ENSP00000509770.1:p.Val436=
ENST00000693763.1:n.2419T=
ENST00000245407.8:c.1259T= MANE Select	ENSP00000245407.3:p.Val420=
ENST00000245407.7:c.1259T=	ENSP00000245407.3:p.Val420=
ENST00000435065.6:c.1331T=	ENSP00000402760.2:p.Val444=
ENST00000447841.5:c.112-1537T=
ENST00000448810.5:c.521T=
ENST00000461013.5:n.8681T=
ENST00000475308.1:n.1937T=
ENST00000479605.5:n.362T=
NM_001308122.1:c.1331T=	NP_001295051.1:p.Val444=
NM_003060.3:c.1259T=	NP_003051.1:p.Val420=
XM_011543590.1:c.641T=	XP_011541892.1:p.Val214=
XR_427718.1:n.1619T=
XR_948290.1:n.1394-1537T=
XR_948291.1:n.1613T=
XM_011543590.2:c.641T=	XP_011541892.1:p.Val214=
XM_017009778.2:c.731T=	XP_016865267.1:p.Val244=
XR_001742215.1:n.1514T=
XR_001742216.1:n.1533T=
XR_427718.2:n.1619T=
XR_948290.2:n.1394-1537T=
XR_948291.2:n.1613T=
NM_003060.4:c.1259T= MANE Select	NP_003051.1:p.Val420=
NM_001308122.2:c.1331T=	NP_001295051.1:p.Val444=