Canonical Allele Identifier: CA360804758

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131719915A>T (hg19) ; chr5:g.132384223A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384223A>T , CM000667.2:g.132384223A>T	GRCh38
NC_000005.9:g.131719915A>T , CM000667.1:g.131719915A>T	GRCh37
NC_000005.8:g.131747814A>T	NCBI36
NG_008982.1:g.19515A>T
NG_008982.2:g.19520A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.574A>T	ENSP00000388838.2:p.Asn192Tyr
ENST00000435065.7:c.646A>T	ENSP00000402760.2:p.Asn216Tyr
ENST00000448810.6:c.574A>T	ENSP00000401860.2:p.Asn192Tyr
ENST00000686757.1:c.574A>T	ENSP00000510721.1:p.Asn192Tyr
ENST00000687740.1:n.708A>T
ENST00000688151.1:n.1753A>T
ENST00000689271.1:c.574A>T	ENSP00000510797.1:p.Asn192Tyr
ENST00000690900.1:c.574A>T	ENSP00000510703.1:p.Asn192Tyr
ENST00000692355.1:c.126A>T
ENST00000692413.1:c.574A>T	ENSP00000509374.1:p.Asn192Tyr
ENST00000692825.1:c.642A>T	ENSP00000509447.1:n.642A>T
ENST00000693308.1:c.574A>T	ENSP00000509770.1:p.Asn192Tyr
ENST00000693763.1:n.708A>T
ENST00000245407.8:c.574A>T MANE Select	ENSP00000245407.3:p.Asn192Tyr
ENST00000245407.7:c.574A>T	ENSP00000245407.3:p.Asn192Tyr
ENST00000415928.5:c.343A>T	ENSP00000388838.1:p.Asn115Tyr
ENST00000435065.6:c.646A>T	ENSP00000402760.2:p.Asn216Tyr
ENST00000437841.6:c.394-1105A>T	ENSP00000400553.1:n.394-1105A>T
ENST00000461013.5:n.7996A>T
NM_001308122.1:c.646A>T	NP_001295051.1:p.Asn216Tyr
NM_003060.3:c.574A>T	NP_003051.1:p.Asn192Tyr
XM_011543590.1:c.-58A>T	XP_011541892.1:n.-58A>T
XR_427718.1:n.915A>T
XR_948290.1:n.915A>T
XR_948291.1:n.915A>T
XM_011543590.2:c.-58A>T	XP_011541892.1:n.-58A>T
XM_017009778.2:c.46A>T	XP_016865267.1:p.Asn16Tyr
XR_001742215.1:n.915A>T
XR_001742216.1:n.915A>T
XR_427718.2:n.915A>T
XR_948290.2:n.915A>T
XR_948291.2:n.915A>T
NM_003060.4:c.574A>T MANE Select	NP_003051.1:p.Asn192Tyr
NM_001308122.2:c.646A>T	NP_001295051.1:p.Asn216Tyr