Canonical Allele Identifier: CA360809789

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729421A>T (hg19) ; chr5:g.132393729A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393729A>T , CM000667.2:g.132393729A>T	GRCh38
NC_000005.9:g.131729421A>T , CM000667.1:g.131729421A>T	GRCh37
NC_000005.8:g.131757320A>T	NCBI36
NG_008982.1:g.29021A>T
NG_008982.2:g.29026A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-456A>T	ENSP00000388838.2:n.1292-456A>T
ENST00000435065.7:c.1576A>T	ENSP00000402760.2:p.Thr526Ser
ENST00000448810.6:c.*356A>T	ENSP00000401860.2:n.*356A>T
ENST00000685543.1:n.1645A>T
ENST00000686757.1:c.*668A>T	ENSP00000510721.1:n.*668A>T
ENST00000686868.1:n.496A>T
ENST00000687740.1:n.4189A>T
ENST00000688151.1:n.2814A>T
ENST00000689271.1:c.1351A>T	ENSP00000510797.1:p.Thr451Ser
ENST00000690900.1:c.*668A>T	ENSP00000510703.1:n.*668A>T
ENST00000692212.1:n.4644A>T
ENST00000692355.1:c.757A>T
ENST00000692413.1:c.1486A>T	ENSP00000509374.1:p.Thr496Ser
ENST00000692825.1:c.1572A>T	ENSP00000509447.1:n.1572A>T
ENST00000693308.1:c.1552A>T	ENSP00000509770.1:p.Thr518Ser
ENST00000693763.1:n.2664A>T
ENST00000245407.8:c.1504A>T MANE Select	ENSP00000245407.3:p.Thr502Ser
ENST00000245407.7:c.1504A>T	ENSP00000245407.3:p.Thr502Ser
ENST00000435065.6:c.1576A>T	ENSP00000402760.2:p.Thr526Ser
ENST00000447841.5:c.348A>T
ENST00000448810.5:c.766A>T
ENST00000461013.5:n.8926A>T
ENST00000475308.1:n.2182A>T
NM_001308122.1:c.1576A>T	NP_001295051.1:p.Thr526Ser
NM_003060.3:c.1504A>T	NP_003051.1:p.Thr502Ser
XM_011543590.1:c.886A>T	XP_011541892.1:p.Thr296Ser
XR_948290.1:n.1630A>T
XM_011543590.2:c.886A>T	XP_011541892.1:p.Thr296Ser
XM_017009778.2:c.976A>T	XP_016865267.1:p.Thr326Ser
XR_001742215.1:n.1759A>T
XR_001742216.1:n.1778A>T
XR_427718.2:n.1864A>T
XR_948290.2:n.1630A>T
XR_948291.2:n.1858A>T
NM_003060.4:c.1504A>T MANE Select	NP_003051.1:p.Thr502Ser
NM_001308122.2:c.1576A>T	NP_001295051.1:p.Thr526Ser