Canonical Allele Identifier: CA446340265

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726595A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390903A>T , CM000667.2:g.132390903A>T	GRCh38
NC_000005.9:g.131726595A>T , CM000667.1:g.131726595A>T	GRCh37
NC_000005.8:g.131754494A>T	NCBI36
NG_008982.1:g.26195A>T
NG_008982.2:g.26200A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1107A>T	ENSP00000388838.2:p.Pro369=
ENST00000435065.7:c.1338A>T	ENSP00000402760.2:p.Pro446=
ENST00000448810.6:c.*118A>T	ENSP00000401860.2:n.*118A>T
ENST00000685543.1:n.1407A>T
ENST00000686757.1:c.*430A>T	ENSP00000510721.1:n.*430A>T
ENST00000687740.1:n.3951A>T
ENST00000688151.1:n.2576A>T
ENST00000689271.1:c.1113A>T	ENSP00000510797.1:p.Pro371=
ENST00000690900.1:c.*430A>T	ENSP00000510703.1:n.*430A>T
ENST00000692212.1:n.2878A>T
ENST00000692355.1:c.519A>T
ENST00000692413.1:c.1248A>T	ENSP00000509374.1:p.Pro416=
ENST00000692825.1:c.1334A>T	ENSP00000509447.1:n.1334A>T
ENST00000693308.1:c.1314A>T	ENSP00000509770.1:p.Pro438=
ENST00000693763.1:n.2426A>T
ENST00000245407.8:c.1266A>T MANE Select	ENSP00000245407.3:p.Pro422=
ENST00000245407.7:c.1266A>T	ENSP00000245407.3:p.Pro422=
ENST00000435065.6:c.1338A>T	ENSP00000402760.2:p.Pro446=
ENST00000447841.5:c.112-1530A>T
ENST00000448810.5:c.528A>T
ENST00000461013.5:n.8688A>T
ENST00000475308.1:n.1944A>T
ENST00000479605.5:n.369A>T
NM_001308122.1:c.1338A>T	NP_001295051.1:p.Pro446=
NM_003060.3:c.1266A>T	NP_003051.1:p.Pro422=
XM_011543590.1:c.648A>T	XP_011541892.1:p.Pro216=
XR_427718.1:n.1626A>T
XR_948290.1:n.1394-1530A>T
XR_948291.1:n.1620A>T
XM_011543590.2:c.648A>T	XP_011541892.1:p.Pro216=
XM_017009778.2:c.738A>T	XP_016865267.1:p.Pro246=
XR_001742215.1:n.1521A>T
XR_001742216.1:n.1540A>T
XR_427718.2:n.1626A>T
XR_948290.2:n.1394-1530A>T
XR_948291.2:n.1620A>T
NM_003060.4:c.1266A>T MANE Select	NP_003051.1:p.Pro422=
NM_001308122.2:c.1338A>T	NP_001295051.1:p.Pro446=