Canonical Allele Identifier: CA2675199433
Gene: SLC22A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393627C>A , CM000667.2:g.132393627C>A GRCh38
NC_000005.9:g.131729319C>A , CM000667.1:g.131729319C>A GRCh37
NC_000005.8:g.131757218C>A NCBI36
NG_008982.1:g.28919C>A
NG_008982.2:g.28924C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-558C>A ENSP00000388838.2:n.1292-558C>A
ENST00000435065.7:c.1523-49C>A ENSP00000402760.2:n.1523-49C>A
ENST00000448810.6:c.*303-49C>A ENSP00000401860.2:n.*303-49C>A
ENST00000685543.1:n.1592-49C>A
ENST00000686757.1:c.*615-49C>A ENSP00000510721.1:n.*615-49C>A
ENST00000686868.1:n.394C>A
ENST00000687740.1:n.4136-49C>A
ENST00000688151.1:n.2761-49C>A
ENST00000689271.1:c.1298-49C>A ENSP00000510797.1:n.1298-49C>A
ENST00000690900.1:c.*615-49C>A ENSP00000510703.1:n.*615-49C>A
ENST00000692212.1:n.4591-49C>A
ENST00000692355.1:c.704-49C>A
ENST00000692413.1:c.1433-49C>A ENSP00000509374.1:n.1433-49C>A
ENST00000692825.1:c.1519-49C>A ENSP00000509447.1:n.1519-49C>A
ENST00000693308.1:c.1499-49C>A ENSP00000509770.1:n.1499-49C>A
ENST00000693763.1:n.2611-49C>A
ENST00000245407.8:c.1451-49C>A MANE Select ENSP00000245407.3:n.1451-49C>A
ENST00000245407.7:c.1451-49C>A ENSP00000245407.3:n.1451-49C>A
ENST00000435065.6:c.1523-49C>A ENSP00000402760.2:n.1523-49C>A
ENST00000447841.5:c.295-49C>A
ENST00000448810.5:c.713-49C>A
ENST00000461013.5:n.8873-49C>A
ENST00000475308.1:n.2129-49C>A
ENST00000479605.5:n.554-49C>A
NM_001308122.1:c.1523-49C>A NP_001295051.1:n.1523-49C>A
NM_003060.3:c.1451-49C>A NP_003051.1:n.1451-49C>A
XM_011543590.1:c.833-49C>A XP_011541892.1:n.833-49C>A
XR_948290.1:n.1577-49C>A
XM_011543590.2:c.833-49C>A XP_011541892.1:n.833-49C>A
XM_017009778.2:c.923-49C>A XP_016865267.1:n.923-49C>A
XR_001742215.1:n.1706-49C>A
XR_001742216.1:n.1725-49C>A
XR_427718.2:n.1811-49C>A
XR_948290.2:n.1577-49C>A
XR_948291.2:n.1805-49C>A
NM_003060.4:c.1451-49C>A MANE Select NP_003051.1:n.1451-49C>A
NM_001308122.2:c.1523-49C>A NP_001295051.1:n.1523-49C>A