Canonical Allele Identifier: CA446338369

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726484A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390792A>T , CM000667.2:g.132390792A>T	GRCh38
NC_000005.9:g.131726484A>T , CM000667.1:g.131726484A>T	GRCh37
NC_000005.8:g.131754383A>T	NCBI36
NG_008982.1:g.26084A>T
NG_008982.2:g.26089A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.996A>T	ENSP00000388838.2:p.Pro332=
ENST00000435065.7:c.1227A>T	ENSP00000402760.2:p.Pro409=
ENST00000448810.6:c.*7A>T	ENSP00000401860.2:n.*7A>T
ENST00000685543.1:n.1296A>T
ENST00000686757.1:c.*319A>T	ENSP00000510721.1:n.*319A>T
ENST00000687740.1:n.3840A>T
ENST00000688151.1:n.2465A>T
ENST00000689271.1:c.1002A>T	ENSP00000510797.1:p.Pro334=
ENST00000690900.1:c.*319A>T	ENSP00000510703.1:n.*319A>T
ENST00000692212.1:n.2767A>T
ENST00000692355.1:c.408A>T
ENST00000692413.1:c.1137A>T	ENSP00000509374.1:p.Pro379=
ENST00000692825.1:c.1223A>T	ENSP00000509447.1:n.1223A>T
ENST00000693308.1:c.1203A>T	ENSP00000509770.1:p.Pro401=
ENST00000693763.1:n.2315A>T
ENST00000245407.8:c.1155A>T MANE Select	ENSP00000245407.3:p.Pro385=
ENST00000245407.7:c.1155A>T	ENSP00000245407.3:p.Pro385=
ENST00000435065.6:c.1227A>T	ENSP00000402760.2:p.Pro409=
ENST00000447841.5:c.112-1641A>T
ENST00000448810.5:c.417A>T
ENST00000461013.5:n.8577A>T
ENST00000475308.1:n.1833A>T
ENST00000479605.5:n.258A>T
NM_001308122.1:c.1227A>T	NP_001295051.1:p.Pro409=
NM_003060.3:c.1155A>T	NP_003051.1:p.Pro385=
XM_011543590.1:c.537A>T	XP_011541892.1:p.Pro179=
XR_427718.1:n.1515A>T
XR_948290.1:n.1394-1641A>T
XR_948291.1:n.1509A>T
XM_011543590.2:c.537A>T	XP_011541892.1:p.Pro179=
XM_017009778.2:c.627A>T	XP_016865267.1:p.Pro209=
XR_001742215.1:n.1410A>T
XR_001742216.1:n.1429A>T
XR_427718.2:n.1515A>T
XR_948290.2:n.1394-1641A>T
XR_948291.2:n.1509A>T
NM_003060.4:c.1155A>T MANE Select	NP_003051.1:p.Pro385=
NM_001308122.2:c.1227A>T	NP_001295051.1:p.Pro409=