Canonical Allele Identifier: CA360809932

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729461C>A (hg19) ; chr5:g.132393769C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393769C>A , CM000667.2:g.132393769C>A	GRCh38
NC_000005.9:g.131729461C>A , CM000667.1:g.131729461C>A	GRCh37
NC_000005.8:g.131757360C>A	NCBI36
NG_008982.1:g.29061C>A
NG_008982.2:g.29066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-416C>A	ENSP00000388838.2:n.1292-416C>A
ENST00000435065.7:c.1616C>A	ENSP00000402760.2:p.Thr539Asn
ENST00000448810.6:c.*396C>A	ENSP00000401860.2:n.*396C>A
ENST00000685543.1:n.1685C>A
ENST00000686757.1:c.*708C>A	ENSP00000510721.1:n.*708C>A
ENST00000686868.1:n.536C>A
ENST00000687740.1:n.4229C>A
ENST00000688151.1:n.2854C>A
ENST00000689271.1:c.1391C>A	ENSP00000510797.1:p.Thr464Asn
ENST00000690900.1:c.*708C>A	ENSP00000510703.1:n.*708C>A
ENST00000692212.1:n.4684C>A
ENST00000692355.1:c.797C>A
ENST00000692413.1:c.1526C>A	ENSP00000509374.1:p.Thr509Asn
ENST00000692825.1:c.1612C>A	ENSP00000509447.1:n.1612C>A
ENST00000693308.1:c.1592C>A	ENSP00000509770.1:p.Thr531Asn
ENST00000693763.1:n.2704C>A
ENST00000245407.8:c.1544C>A MANE Select	ENSP00000245407.3:p.Thr515Asn
ENST00000245407.7:c.1544C>A	ENSP00000245407.3:p.Thr515Asn
ENST00000435065.6:c.1616C>A	ENSP00000402760.2:p.Thr539Asn
ENST00000447841.5:c.388C>A
ENST00000448810.5:c.806C>A
ENST00000461013.5:n.8966C>A
ENST00000475308.1:n.2222C>A
NM_001308122.1:c.1616C>A	NP_001295051.1:p.Thr539Asn
NM_003060.3:c.1544C>A	NP_003051.1:p.Thr515Asn
XM_011543590.1:c.926C>A	XP_011541892.1:p.Thr309Asn
XR_948290.1:n.1670C>A
XM_011543590.2:c.926C>A	XP_011541892.1:p.Thr309Asn
XM_017009778.2:c.1016C>A	XP_016865267.1:p.Thr339Asn
XR_001742215.1:n.1799C>A
XR_001742216.1:n.1818C>A
XR_427718.2:n.1904C>A
XR_948290.2:n.1670C>A
XR_948291.2:n.1898C>A
NM_003060.4:c.1544C>A MANE Select	NP_003051.1:p.Thr515Asn
NM_001308122.2:c.1616C>A	NP_001295051.1:p.Thr539Asn