Canonical Allele Identifier: CA360803214

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131713861C>A (hg19) ; chr5:g.132378169C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132378169C>A , CM000667.2:g.132378169C>A	GRCh38
NC_000005.9:g.131713861C>A , CM000667.1:g.131713861C>A	GRCh37
NC_000005.8:g.131741760C>A	NCBI36
NG_008982.1:g.13461C>A
NG_008982.2:g.13466C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.394-209C>A	ENSP00000388838.2:n.394-209C>A
ENST00000435065.7:c.399C>A	ENSP00000402760.2:p.Asp133Glu
ENST00000448810.6:c.394-209C>A	ENSP00000401860.2:n.394-209C>A
ENST00000686757.1:c.394-209C>A	ENSP00000510721.1:n.394-209C>A
ENST00000687740.1:n.528-209C>A
ENST00000689271.1:c.394-209C>A	ENSP00000510797.1:n.394-209C>A
ENST00000690900.1:c.394-209C>A	ENSP00000510703.1:n.394-209C>A
ENST00000692413.1:c.394-209C>A	ENSP00000509374.1:n.394-209C>A
ENST00000692825.1:c.395C>A	ENSP00000509447.1:p.Thr132Lys
ENST00000693308.1:c.394-209C>A	ENSP00000509770.1:n.394-209C>A
ENST00000693763.1:n.528-209C>A
ENST00000245407.8:c.394-209C>A MANE Select	ENSP00000245407.3:n.394-209C>A
ENST00000245407.7:c.394-209C>A	ENSP00000245407.3:n.394-209C>A
ENST00000415928.5:c.96C>A	ENSP00000388838.1:p.Asp32Glu
ENST00000435065.6:c.399C>A	ENSP00000402760.2:p.Asp133Glu
ENST00000437841.6:c.394-7159C>A	ENSP00000400553.1:n.394-7159C>A
ENST00000461013.5:n.2084C>A
NM_001308122.1:c.399C>A	NP_001295051.1:p.Asp133Glu
NM_003060.3:c.394-209C>A	NP_003051.1:n.394-209C>A
XR_427718.1:n.668C>A
XR_948290.1:n.668C>A
XR_948291.1:n.668C>A
XM_011543590.2:c.-238-209C>A	XP_011541892.1:n.-238-209C>A
XM_017009778.2:c.-31-5978C>A	XP_016865267.1:n.-31-5978C>A
XR_001742215.1:n.668C>A
XR_001742216.1:n.668C>A
XR_427718.2:n.668C>A
XR_948290.2:n.668C>A
XR_948291.2:n.668C>A
NM_003060.4:c.394-209C>A MANE Select	NP_003051.1:n.394-209C>A
NM_001308122.2:c.399C>A	NP_001295051.1:p.Asp133Glu