Canonical Allele Identifier: CA360804934

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132385327-G-A
• MyVariant Identifiers: chr5:g.131721019G>A (hg19) ; chr5:g.132385327G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385327G>A , CM000667.2:g.132385327G>A	GRCh38
NC_000005.9:g.131721019G>A , CM000667.1:g.131721019G>A	GRCh37
NC_000005.8:g.131748918G>A	NCBI36
NG_008982.1:g.20619G>A
NG_008982.2:g.20624G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1013G>A	ENSP00000388838.2:n.665+1013G>A
ENST00000435065.7:c.725-1G>A	ENSP00000402760.2:n.725-1G>A
ENST00000448810.6:c.653-1G>A	ENSP00000401860.2:n.653-1G>A
ENST00000686757.1:c.672-1G>A	ENSP00000510721.1:n.672-1G>A
ENST00000687740.1:n.1812G>A
ENST00000688151.1:n.1845-1G>A
ENST00000689271.1:c.671+1007G>A	ENSP00000510797.1:n.671+1007G>A
ENST00000690900.1:c.672-49G>A	ENSP00000510703.1:n.672-49G>A
ENST00000692212.1:n.478G>A
ENST00000692355.1:c.204+1026G>A
ENST00000692413.1:c.672-1G>A	ENSP00000509374.1:n.672-1G>A
ENST00000692825.1:c.721-1G>A	ENSP00000509447.1:n.721-1G>A
ENST00000693308.1:c.666-1G>A	ENSP00000509770.1:n.666-1G>A
ENST00000693763.1:n.1812G>A
ENST00000245407.8:c.653-1G>A MANE Select	ENSP00000245407.3:n.653-1G>A
ENST00000245407.7:c.653-1G>A	ENSP00000245407.3:n.653-1G>A
ENST00000415928.5:c.422-1G>A	ENSP00000388838.1:n.422-1G>A
ENST00000435065.6:c.725-1G>A	ENSP00000402760.2:n.725-1G>A
ENST00000437841.6:c.394-1G>A	ENSP00000400553.1:n.394-1G>A
ENST00000461013.5:n.8075-1G>A
NM_001308122.1:c.725-1G>A	NP_001295051.1:n.725-1G>A
NM_003060.3:c.653-1G>A	NP_003051.1:n.653-1G>A
XM_011543590.1:c.35-1G>A	XP_011541892.1:n.35-1G>A
XR_427718.1:n.1013-1G>A
XR_948290.1:n.994-1G>A
XR_948291.1:n.1007-1G>A
XM_011543590.2:c.35-1G>A	XP_011541892.1:n.35-1G>A
XM_017009778.2:c.125-1G>A	XP_016865267.1:n.125-1G>A
XR_001742215.1:n.994-1G>A
XR_001742216.1:n.1013-1G>A
XR_427718.2:n.1013-1G>A
XR_948290.2:n.994-1G>A
XR_948291.2:n.1007-1G>A
NM_003060.4:c.653-1G>A MANE Select	NP_003051.1:n.653-1G>A
NM_001308122.2:c.725-1G>A	NP_001295051.1:n.725-1G>A