Canonical Allele Identifier: CA2675200927
Gene: SLC22A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132386963C>A , CM000667.2:g.132386963C>A GRCh38
NC_000005.9:g.131722655C>A , CM000667.1:g.131722655C>A GRCh37
NC_000005.8:g.131750554C>A NCBI36
NG_008982.1:g.22255C>A
NG_008982.2:g.22260C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.666-62C>A ENSP00000388838.2:n.666-62C>A
ENST00000435065.7:c.897-62C>A ENSP00000402760.2:n.897-62C>A
ENST00000448810.6:c.825-62C>A ENSP00000401860.2:n.825-62C>A
ENST00000686757.1:c.844-62C>A ENSP00000510721.1:n.844-62C>A
ENST00000687740.1:n.3448C>A
ENST00000688151.1:n.2135-62C>A
ENST00000689271.1:c.672-62C>A ENSP00000510797.1:n.672-62C>A
ENST00000690900.1:c.796-62C>A ENSP00000510703.1:n.796-62C>A
ENST00000692212.1:n.769-62C>A
ENST00000692355.1:c.205-1958C>A
ENST00000692413.1:c.844-99C>A ENSP00000509374.1:n.844-99C>A
ENST00000692825.1:c.893-62C>A ENSP00000509447.1:n.893-62C>A
ENST00000693308.1:c.838-27C>A ENSP00000509770.1:n.838-27C>A
ENST00000693763.1:n.1985-62C>A
ENST00000245407.8:c.825-62C>A MANE Select ENSP00000245407.3:n.825-62C>A
ENST00000245407.7:c.825-62C>A ENSP00000245407.3:n.825-62C>A
ENST00000415928.5:c.594-62C>A ENSP00000388838.1:n.594-62C>A
ENST00000435065.6:c.897-62C>A ENSP00000402760.2:n.897-62C>A
ENST00000437841.6:c.*140-62C>A ENSP00000400553.1:n.*140-62C>A
ENST00000448810.5:c.173-62C>A
ENST00000461013.5:n.8247-62C>A
NM_001308122.1:c.897-62C>A NP_001295051.1:n.897-62C>A
NM_003060.3:c.825-62C>A NP_003051.1:n.825-62C>A
XM_011543590.1:c.207-62C>A XP_011541892.1:n.207-62C>A
XR_427718.1:n.1185-62C>A
XR_948290.1:n.1166-62C>A
XR_948291.1:n.1179-62C>A
XM_011543590.2:c.207-62C>A XP_011541892.1:n.207-62C>A
XM_017009778.2:c.297-62C>A XP_016865267.1:n.297-62C>A
XR_001742215.1:n.1166-62C>A
XR_001742216.1:n.1185-62C>A
XR_427718.2:n.1185-62C>A
XR_948290.2:n.1166-62C>A
XR_948291.2:n.1179-62C>A
NM_003060.4:c.825-62C>A MANE Select NP_003051.1:n.825-62C>A
NM_001308122.2:c.897-62C>A NP_001295051.1:n.897-62C>A