Canonical Allele Identifier: CA360807736

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726532T>G (hg19) ; chr5:g.132390840T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390840T>G , CM000667.2:g.132390840T>G	GRCh38
NC_000005.9:g.131726532T>G , CM000667.1:g.131726532T>G	GRCh37
NC_000005.8:g.131754431T>G	NCBI36
NG_008982.1:g.26132T>G
NG_008982.2:g.26137T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1044T>G	ENSP00000388838.2:p.Tyr348Ter
ENST00000435065.7:c.1275T>G	ENSP00000402760.2:p.Tyr425Ter
ENST00000448810.6:c.*55T>G	ENSP00000401860.2:n.*55T>G
ENST00000685543.1:n.1344T>G
ENST00000686757.1:c.*367T>G	ENSP00000510721.1:n.*367T>G
ENST00000687740.1:n.3888T>G
ENST00000688151.1:n.2513T>G
ENST00000689271.1:c.1050T>G	ENSP00000510797.1:p.Tyr350Ter
ENST00000690900.1:c.*367T>G	ENSP00000510703.1:n.*367T>G
ENST00000692212.1:n.2815T>G
ENST00000692355.1:c.456T>G
ENST00000692413.1:c.1185T>G	ENSP00000509374.1:p.Tyr395Ter
ENST00000692825.1:c.1271T>G	ENSP00000509447.1:n.1271T>G
ENST00000693308.1:c.1251T>G	ENSP00000509770.1:p.Tyr417Ter
ENST00000693763.1:n.2363T>G
ENST00000245407.8:c.1203T>G MANE Select	ENSP00000245407.3:p.Tyr401Ter
ENST00000245407.7:c.1203T>G	ENSP00000245407.3:p.Tyr401Ter
ENST00000435065.6:c.1275T>G	ENSP00000402760.2:p.Tyr425Ter
ENST00000447841.5:c.112-1593T>G
ENST00000448810.5:c.465T>G
ENST00000461013.5:n.8625T>G
ENST00000475308.1:n.1881T>G
ENST00000479605.5:n.306T>G
NM_001308122.1:c.1275T>G	NP_001295051.1:p.Tyr425Ter
NM_003060.3:c.1203T>G	NP_003051.1:p.Tyr401Ter
XM_011543590.1:c.585T>G	XP_011541892.1:p.Tyr195Ter
XR_427718.1:n.1563T>G
XR_948290.1:n.1394-1593T>G
XR_948291.1:n.1557T>G
XM_011543590.2:c.585T>G	XP_011541892.1:p.Tyr195Ter
XM_017009778.2:c.675T>G	XP_016865267.1:p.Tyr225Ter
XR_001742215.1:n.1458T>G
XR_001742216.1:n.1477T>G
XR_427718.2:n.1563T>G
XR_948290.2:n.1394-1593T>G
XR_948291.2:n.1557T>G
NM_003060.4:c.1203T>G MANE Select	NP_003051.1:p.Tyr401Ter
NM_001308122.2:c.1275T>G	NP_001295051.1:p.Tyr425Ter