Canonical Allele Identifier: CA1583149744
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390644_132390645delinsAG , CM000667.2:g.132390644_132390645delinsAG GRCh38
NC_000005.9:g.131726336_131726337delinsAG , CM000667.1:g.131726336_131726337delinsAG GRCh37
NC_000005.8:g.131754235_131754236delinsAG NCBI36
NG_008982.1:g.25936_25937delinsAG
NG_008982.2:g.25941_25942delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.894-46_894-45delinsAG ENSP00000388838.2:n.894-46_894-45delinsAG...
ENST00000435065.7:c.1125-46_1125-45delinsAG ENSP00000402760.2:n.1125-46_1125-45delins...
ENST00000448810.6:c.1053-132_1053-131delinsAG ENSP00000401860.2:n.1053-132_1053-131deli...
ENST00000685543.1:n.1194-46_1194-45delinsAG
ENST00000686757.1:c.*217-46_*217-45delinsAG ENSP00000510721.1:n.*217-46_*217-45delins...
ENST00000687740.1:n.3738-46_3738-45delinsAG
ENST00000688151.1:n.2363-46_2363-45delinsAG
ENST00000689271.1:c.900-46_900-45delinsAG ENSP00000510797.1:n.900-46_900-45delinsAG...
ENST00000690900.1:c.*217-46_*217-45delinsAG ENSP00000510703.1:n.*217-46_*217-45delins...
ENST00000692212.1:n.2619_2620delinsAG
ENST00000692355.1:c.306-46_306-45delinsAG
ENST00000692413.1:c.1035-46_1035-45delinsAG ENSP00000509374.1:n.1035-46_1035-45delins...
ENST00000692825.1:c.1121-46_1121-45delinsAG ENSP00000509447.1:n.1121-46_1121-45delins...
ENST00000693308.1:c.1101-46_1101-45delinsAG ENSP00000509770.1:n.1101-46_1101-45delins...
ENST00000693763.1:n.2213-46_2213-45delinsAG
ENST00000245407.8:c.1053-46_1053-45delinsAG MANE Select ENSP00000245407.3:n.1053-46_1053-45delins...
ENST00000245407.7:c.1053-46_1053-45delinsAG ENSP00000245407.3:n.1053-46_1053-45delins...
ENST00000435065.6:c.1125-46_1125-45delinsAG ENSP00000402760.2:n.1125-46_1125-45delins...
ENST00000447841.5:c.111+1623_111+1624delinsAG
ENST00000448810.5:c.401-132_401-131delinsAG
ENST00000461013.5:n.8475-46_8475-45delinsAG
ENST00000475308.1:n.1685_1686delinsAG
ENST00000479605.5:n.156-46_156-45delinsAG
NM_001308122.1:c.1125-46_1125-45delinsAG NP_001295051.1:n.1125-46_1125-45delinsAG
NM_003060.3:c.1053-46_1053-45delinsAG NP_003051.1:n.1053-46_1053-45delinsAG
XM_011543590.1:c.435-46_435-45delinsAG XP_011541892.1:n.435-46_435-45delinsAG
XR_427718.1:n.1413-46_1413-45delinsAG
XR_948290.1:n.1393+1623_1393+1624delinsAG
XR_948291.1:n.1407-46_1407-45delinsAG
XM_011543590.2:c.435-46_435-45delinsAG XP_011541892.1:n.435-46_435-45delinsAG
XM_017009778.2:c.525-46_525-45delinsAG XP_016865267.1:n.525-46_525-45delinsAG
XR_001742215.1:n.1394-132_1394-131delinsAG
XR_001742216.1:n.1413-132_1413-131delinsAG
XR_427718.2:n.1413-46_1413-45delinsAG
XR_948290.2:n.1393+1623_1393+1624delinsAG
XR_948291.2:n.1407-46_1407-45delinsAG
NM_003060.4:c.1053-46_1053-45delinsAG MANE Select NP_003051.1:n.1053-46_1053-45delinsAG
NM_001308122.2:c.1125-46_1125-45delinsAG NP_001295051.1:n.1125-46_1125-45delinsAG