Canonical Allele Identifier: CA360807571

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726452A>G (hg19) ; chr5:g.132390760A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390760A>G , CM000667.2:g.132390760A>G	GRCh38
NC_000005.9:g.131726452A>G , CM000667.1:g.131726452A>G	GRCh37
NC_000005.8:g.131754351A>G	NCBI36
NG_008982.1:g.26052A>G
NG_008982.2:g.26057A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.964A>G	ENSP00000388838.2:p.Asn322Asp
ENST00000435065.7:c.1195A>G	ENSP00000402760.2:p.Asn399Asp
ENST00000448810.6:c.1053-16A>G	ENSP00000401860.2:n.1053-16A>G
ENST00000685543.1:n.1264A>G
ENST00000686757.1:c.*287A>G	ENSP00000510721.1:n.*287A>G
ENST00000687740.1:n.3808A>G
ENST00000688151.1:n.2433A>G
ENST00000689271.1:c.970A>G	ENSP00000510797.1:p.Asn324Asp
ENST00000690900.1:c.*287A>G	ENSP00000510703.1:n.*287A>G
ENST00000692212.1:n.2735A>G
ENST00000692355.1:c.376A>G
ENST00000692413.1:c.1105A>G	ENSP00000509374.1:p.Asn369Asp
ENST00000692825.1:c.1191A>G	ENSP00000509447.1:n.1191A>G
ENST00000693308.1:c.1171A>G	ENSP00000509770.1:p.Asn391Asp
ENST00000693763.1:n.2283A>G
ENST00000245407.8:c.1123A>G MANE Select	ENSP00000245407.3:p.Asn375Asp
ENST00000245407.7:c.1123A>G	ENSP00000245407.3:p.Asn375Asp
ENST00000435065.6:c.1195A>G	ENSP00000402760.2:p.Asn399Asp
ENST00000447841.5:c.112-1673A>G
ENST00000448810.5:c.401-16A>G
ENST00000461013.5:n.8545A>G
ENST00000475308.1:n.1801A>G
ENST00000479605.5:n.226A>G
NM_001308122.1:c.1195A>G	NP_001295051.1:p.Asn399Asp
NM_003060.3:c.1123A>G	NP_003051.1:p.Asn375Asp
XM_011543590.1:c.505A>G	XP_011541892.1:p.Asn169Asp
XR_427718.1:n.1483A>G
XR_948290.1:n.1394-1673A>G
XR_948291.1:n.1477A>G
XM_011543590.2:c.505A>G	XP_011541892.1:p.Asn169Asp
XM_017009778.2:c.595A>G	XP_016865267.1:p.Asn199Asp
XR_001742215.1:n.1394-16A>G
XR_001742216.1:n.1413-16A>G
XR_427718.2:n.1483A>G
XR_948290.2:n.1394-1673A>G
XR_948291.2:n.1477A>G
NM_003060.4:c.1123A>G MANE Select	NP_003051.1:p.Asn375Asp
NM_001308122.2:c.1195A>G	NP_001295051.1:p.Asn399Asp