Canonical Allele Identifier: CA446345329

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729369T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393677T>A , CM000667.2:g.132393677T>A	GRCh38
NC_000005.9:g.131729369T>A , CM000667.1:g.131729369T>A	GRCh37
NC_000005.8:g.131757268T>A	NCBI36
NG_008982.1:g.28969T>A
NG_008982.2:g.28974T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-508T>A	ENSP00000388838.2:n.1292-508T>A
ENST00000435065.7:c.1524T>A	ENSP00000402760.2:p.Gly508=
ENST00000448810.6:c.*304T>A	ENSP00000401860.2:n.*304T>A
ENST00000685543.1:n.1593T>A
ENST00000686757.1:c.*616T>A	ENSP00000510721.1:n.*616T>A
ENST00000686868.1:n.444T>A
ENST00000687740.1:n.4137T>A
ENST00000688151.1:n.2762T>A
ENST00000689271.1:c.1299T>A	ENSP00000510797.1:p.Gly433=
ENST00000690900.1:c.*616T>A	ENSP00000510703.1:n.*616T>A
ENST00000692212.1:n.4592T>A
ENST00000692355.1:c.705T>A
ENST00000692413.1:c.1434T>A	ENSP00000509374.1:p.Gly478=
ENST00000692825.1:c.1520T>A	ENSP00000509447.1:n.1520T>A
ENST00000693308.1:c.1500T>A	ENSP00000509770.1:p.Gly500=
ENST00000693763.1:n.2612T>A
ENST00000245407.8:c.1452T>A MANE Select	ENSP00000245407.3:p.Gly484=
ENST00000245407.7:c.1452T>A	ENSP00000245407.3:p.Gly484=
ENST00000435065.6:c.1524T>A	ENSP00000402760.2:p.Gly508=
ENST00000447841.5:c.296T>A
ENST00000448810.5:c.714T>A
ENST00000461013.5:n.8874T>A
ENST00000475308.1:n.2130T>A
ENST00000479605.5:n.555T>A
NM_001308122.1:c.1524T>A	NP_001295051.1:p.Gly508=
NM_003060.3:c.1452T>A	NP_003051.1:p.Gly484=
XM_011543590.1:c.834T>A	XP_011541892.1:p.Gly278=
XR_948290.1:n.1578T>A
XM_011543590.2:c.834T>A	XP_011541892.1:p.Gly278=
XM_017009778.2:c.924T>A	XP_016865267.1:p.Gly308=
XR_001742215.1:n.1707T>A
XR_001742216.1:n.1726T>A
XR_427718.2:n.1812T>A
XR_948290.2:n.1578T>A
XR_948291.2:n.1806T>A
NM_003060.4:c.1452T>A MANE Select	NP_003051.1:p.Gly484=
NM_001308122.2:c.1524T>A	NP_001295051.1:p.Gly508=