Canonical Allele Identifier: CA446343157

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131728204C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392512C>T , CM000667.2:g.132392512C>T	GRCh38
NC_000005.9:g.131728204C>T , CM000667.1:g.131728204C>T	GRCh37
NC_000005.8:g.131756103C>T	NCBI36
NG_008982.1:g.27804C>T
NG_008982.2:g.27809C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1188C>T	ENSP00000388838.2:p.Tyr396=
ENST00000435065.7:c.1419C>T	ENSP00000402760.2:p.Tyr473=
ENST00000448810.6:c.*199C>T	ENSP00000401860.2:n.*199C>T
ENST00000685543.1:n.1488C>T
ENST00000686757.1:c.*511C>T	ENSP00000510721.1:n.*511C>T
ENST00000687740.1:n.4032C>T
ENST00000688151.1:n.2657C>T
ENST00000689271.1:c.1194C>T	ENSP00000510797.1:p.Tyr398=
ENST00000690900.1:c.*511C>T	ENSP00000510703.1:n.*511C>T
ENST00000692212.1:n.4487C>T
ENST00000692355.1:c.600C>T
ENST00000692413.1:c.1329C>T	ENSP00000509374.1:p.Tyr443=
ENST00000692825.1:c.1415C>T	ENSP00000509447.1:n.1415C>T
ENST00000693308.1:c.1395C>T	ENSP00000509770.1:p.Tyr465=
ENST00000693763.1:n.2507C>T
ENST00000245407.8:c.1347C>T MANE Select	ENSP00000245407.3:p.Tyr449=
ENST00000245407.7:c.1347C>T	ENSP00000245407.3:p.Tyr449=
ENST00000435065.6:c.1419C>T	ENSP00000402760.2:p.Tyr473=
ENST00000447841.5:c.191C>T
ENST00000448810.5:c.609C>T
ENST00000461013.5:n.8769C>T
ENST00000475308.1:n.2025C>T
ENST00000479605.5:n.450C>T
NM_001308122.1:c.1419C>T	NP_001295051.1:p.Tyr473=
NM_003060.3:c.1347C>T	NP_003051.1:p.Tyr449=
XM_011543590.1:c.729C>T	XP_011541892.1:p.Tyr243=
XR_948290.1:n.1473C>T
XM_011543590.2:c.729C>T	XP_011541892.1:p.Tyr243=
XM_017009778.2:c.819C>T	XP_016865267.1:p.Tyr273=
XR_001742215.1:n.1602C>T
XR_001742216.1:n.1621C>T
XR_427718.2:n.1707C>T
XR_948290.2:n.1473C>T
XR_948291.2:n.1701C>T
NM_003060.4:c.1347C>T MANE Select	NP_003051.1:p.Tyr449=
NM_001308122.2:c.1419C>T	NP_001295051.1:p.Tyr473=