Canonical Allele Identifier: CA2675203460

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132390291-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390291T>C , CM000667.2:g.132390291T>C	GRCh38
NC_000005.9:g.131725983T>C , CM000667.1:g.131725983T>C	GRCh37
NC_000005.8:g.131753882T>C	NCBI36
NG_008982.1:g.25583T>C
NG_008982.2:g.25588T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-399T>C	ENSP00000388838.2:n.894-399T>C
ENST00000435065.7:c.1125-399T>C	ENSP00000402760.2:n.1125-399T>C
ENST00000448810.6:c.1053-485T>C	ENSP00000401860.2:n.1053-485T>C
ENST00000685543.1:n.1194-399T>C
ENST00000686757.1:c.*217-399T>C	ENSP00000510721.1:n.*217-399T>C
ENST00000687740.1:n.3738-399T>C
ENST00000688151.1:n.2363-399T>C
ENST00000689271.1:c.900-399T>C	ENSP00000510797.1:n.900-399T>C
ENST00000690900.1:c.*217-399T>C	ENSP00000510703.1:n.*217-399T>C
ENST00000692212.1:n.2266T>C
ENST00000692355.1:c.306-399T>C
ENST00000692413.1:c.1035-399T>C	ENSP00000509374.1:n.1035-399T>C
ENST00000692825.1:c.1121-399T>C	ENSP00000509447.1:n.1121-399T>C
ENST00000693308.1:c.1101-399T>C	ENSP00000509770.1:n.1101-399T>C
ENST00000693763.1:n.2213-399T>C
ENST00000245407.8:c.1053-399T>C MANE Select	ENSP00000245407.3:n.1053-399T>C
ENST00000245407.7:c.1053-399T>C	ENSP00000245407.3:n.1053-399T>C
ENST00000435065.6:c.1125-399T>C	ENSP00000402760.2:n.1125-399T>C
ENST00000447841.5:c.111+1270T>C
ENST00000448810.5:c.401-485T>C
ENST00000461013.5:n.8475-399T>C
ENST00000475308.1:n.1332T>C
ENST00000479605.5:n.156-399T>C
NM_001308122.1:c.1125-399T>C	NP_001295051.1:n.1125-399T>C
NM_003060.3:c.1053-399T>C	NP_003051.1:n.1053-399T>C
XM_011543590.1:c.435-399T>C	XP_011541892.1:n.435-399T>C
XR_427718.1:n.1413-399T>C
XR_948290.1:n.1393+1270T>C
XR_948291.1:n.1407-399T>C
XM_011543590.2:c.435-399T>C	XP_011541892.1:n.435-399T>C
XM_017009778.2:c.525-399T>C	XP_016865267.1:n.525-399T>C
XR_001742215.1:n.1394-485T>C
XR_001742216.1:n.1413-485T>C
XR_427718.2:n.1413-399T>C
XR_948290.2:n.1393+1270T>C
XR_948291.2:n.1407-399T>C
NM_003060.4:c.1053-399T>C MANE Select	NP_003051.1:n.1053-399T>C
NM_001308122.2:c.1125-399T>C	NP_001295051.1:n.1125-399T>C