Canonical Allele Identifier: CA446345867

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729405A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393713A>C , CM000667.2:g.132393713A>C	GRCh38
NC_000005.9:g.131729405A>C , CM000667.1:g.131729405A>C	GRCh37
NC_000005.8:g.131757304A>C	NCBI36
NG_008982.1:g.29005A>C
NG_008982.2:g.29010A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1292-472A>C	ENSP00000388838.2:n.1292-472A>C
ENST00000435065.7:c.1560A>C	ENSP00000402760.2:p.Gly520=
ENST00000448810.6:c.*340A>C	ENSP00000401860.2:n.*340A>C
ENST00000685543.1:n.1629A>C
ENST00000686757.1:c.*652A>C	ENSP00000510721.1:n.*652A>C
ENST00000686868.1:n.480A>C
ENST00000687740.1:n.4173A>C
ENST00000688151.1:n.2798A>C
ENST00000689271.1:c.1335A>C	ENSP00000510797.1:p.Gly445=
ENST00000690900.1:c.*652A>C	ENSP00000510703.1:n.*652A>C
ENST00000692212.1:n.4628A>C
ENST00000692355.1:c.741A>C
ENST00000692413.1:c.1470A>C	ENSP00000509374.1:p.Gly490=
ENST00000692825.1:c.1556A>C	ENSP00000509447.1:n.1556A>C
ENST00000693308.1:c.1536A>C	ENSP00000509770.1:p.Gly512=
ENST00000693763.1:n.2648A>C
ENST00000245407.8:c.1488A>C MANE Select	ENSP00000245407.3:p.Gly496=
ENST00000245407.7:c.1488A>C	ENSP00000245407.3:p.Gly496=
ENST00000435065.6:c.1560A>C	ENSP00000402760.2:p.Gly520=
ENST00000447841.5:c.332A>C
ENST00000448810.5:c.750A>C
ENST00000461013.5:n.8910A>C
ENST00000475308.1:n.2166A>C
NM_001308122.1:c.1560A>C	NP_001295051.1:p.Gly520=
NM_003060.3:c.1488A>C	NP_003051.1:p.Gly496=
XM_011543590.1:c.870A>C	XP_011541892.1:p.Gly290=
XR_948290.1:n.1614A>C
XM_011543590.2:c.870A>C	XP_011541892.1:p.Gly290=
XM_017009778.2:c.960A>C	XP_016865267.1:p.Gly320=
XR_001742215.1:n.1743A>C
XR_001742216.1:n.1762A>C
XR_427718.2:n.1848A>C
XR_948290.2:n.1614A>C
XR_948291.2:n.1842A>C
NM_003060.4:c.1488A>C MANE Select	NP_003051.1:p.Gly496=
NM_001308122.2:c.1560A>C	NP_001295051.1:p.Gly520=