Canonical Allele Identifier: CA360809835

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729434C>G (hg19) ; chr5:g.132393742C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393742C>G , CM000667.2:g.132393742C>G	GRCh38
NC_000005.9:g.131729434C>G , CM000667.1:g.131729434C>G	GRCh37
NC_000005.8:g.131757333C>G	NCBI36
NG_008982.1:g.29034C>G
NG_008982.2:g.29039C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-443C>G	ENSP00000388838.2:n.1292-443C>G
ENST00000435065.7:c.1589C>G	ENSP00000402760.2:p.Thr530Ser
ENST00000448810.6:c.*369C>G	ENSP00000401860.2:n.*369C>G
ENST00000685543.1:n.1658C>G
ENST00000686757.1:c.*681C>G	ENSP00000510721.1:n.*681C>G
ENST00000686868.1:n.509C>G
ENST00000687740.1:n.4202C>G
ENST00000688151.1:n.2827C>G
ENST00000689271.1:c.1364C>G	ENSP00000510797.1:p.Thr455Ser
ENST00000690900.1:c.*681C>G	ENSP00000510703.1:n.*681C>G
ENST00000692212.1:n.4657C>G
ENST00000692355.1:c.770C>G
ENST00000692413.1:c.1499C>G	ENSP00000509374.1:p.Thr500Ser
ENST00000692825.1:c.1585C>G	ENSP00000509447.1:n.1585C>G
ENST00000693308.1:c.1565C>G	ENSP00000509770.1:p.Thr522Ser
ENST00000693763.1:n.2677C>G
ENST00000245407.8:c.1517C>G MANE Select	ENSP00000245407.3:p.Thr506Ser
ENST00000245407.7:c.1517C>G	ENSP00000245407.3:p.Thr506Ser
ENST00000435065.6:c.1589C>G	ENSP00000402760.2:p.Thr530Ser
ENST00000447841.5:c.361C>G
ENST00000448810.5:c.779C>G
ENST00000461013.5:n.8939C>G
ENST00000475308.1:n.2195C>G
NM_001308122.1:c.1589C>G	NP_001295051.1:p.Thr530Ser
NM_003060.3:c.1517C>G	NP_003051.1:p.Thr506Ser
XM_011543590.1:c.899C>G	XP_011541892.1:p.Thr300Ser
XR_948290.1:n.1643C>G
XM_011543590.2:c.899C>G	XP_011541892.1:p.Thr300Ser
XM_017009778.2:c.989C>G	XP_016865267.1:p.Thr330Ser
XR_001742215.1:n.1772C>G
XR_001742216.1:n.1791C>G
XR_427718.2:n.1877C>G
XR_948290.2:n.1643C>G
XR_948291.2:n.1871C>G
NM_003060.4:c.1517C>G MANE Select	NP_003051.1:p.Thr506Ser
NM_001308122.2:c.1589C>G	NP_001295051.1:p.Thr530Ser