Canonical Allele Identifier: CA2675203774

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132390552-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390552G>T , CM000667.2:g.132390552G>T	GRCh38
NC_000005.9:g.131726244G>T , CM000667.1:g.131726244G>T	GRCh37
NC_000005.8:g.131754143G>T	NCBI36
NG_008982.1:g.25844G>T
NG_008982.2:g.25849G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-138G>T	ENSP00000388838.2:n.894-138G>T
ENST00000435065.7:c.1125-138G>T	ENSP00000402760.2:n.1125-138G>T
ENST00000448810.6:c.1053-224G>T	ENSP00000401860.2:n.1053-224G>T
ENST00000685543.1:n.1194-138G>T
ENST00000686757.1:c.*217-138G>T	ENSP00000510721.1:n.*217-138G>T
ENST00000687740.1:n.3738-138G>T
ENST00000688151.1:n.2363-138G>T
ENST00000689271.1:c.900-138G>T	ENSP00000510797.1:n.900-138G>T
ENST00000690900.1:c.*217-138G>T	ENSP00000510703.1:n.*217-138G>T
ENST00000692212.1:n.2527G>T
ENST00000692355.1:c.306-138G>T
ENST00000692413.1:c.1035-138G>T	ENSP00000509374.1:n.1035-138G>T
ENST00000692825.1:c.1121-138G>T	ENSP00000509447.1:n.1121-138G>T
ENST00000693308.1:c.1101-138G>T	ENSP00000509770.1:n.1101-138G>T
ENST00000693763.1:n.2213-138G>T
ENST00000245407.8:c.1053-138G>T MANE Select	ENSP00000245407.3:n.1053-138G>T
ENST00000245407.7:c.1053-138G>T	ENSP00000245407.3:n.1053-138G>T
ENST00000435065.6:c.1125-138G>T	ENSP00000402760.2:n.1125-138G>T
ENST00000447841.5:c.111+1531G>T
ENST00000448810.5:c.401-224G>T
ENST00000461013.5:n.8475-138G>T
ENST00000475308.1:n.1593G>T
ENST00000479605.5:n.156-138G>T
NM_001308122.1:c.1125-138G>T	NP_001295051.1:n.1125-138G>T
NM_003060.3:c.1053-138G>T	NP_003051.1:n.1053-138G>T
XM_011543590.1:c.435-138G>T	XP_011541892.1:n.435-138G>T
XR_427718.1:n.1413-138G>T
XR_948290.1:n.1393+1531G>T
XR_948291.1:n.1407-138G>T
XM_011543590.2:c.435-138G>T	XP_011541892.1:n.435-138G>T
XM_017009778.2:c.525-138G>T	XP_016865267.1:n.525-138G>T
XR_001742215.1:n.1394-224G>T
XR_001742216.1:n.1413-224G>T
XR_427718.2:n.1413-138G>T
XR_948290.2:n.1393+1531G>T
XR_948291.2:n.1407-138G>T
NM_003060.4:c.1053-138G>T MANE Select	NP_003051.1:n.1053-138G>T
NM_001308122.2:c.1125-138G>T	NP_001295051.1:n.1125-138G>T