Canonical Allele Identifier: CA2675200986

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132386982-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132386982G>C , CM000667.2:g.132386982G>C	GRCh38
NC_000005.9:g.131722674G>C , CM000667.1:g.131722674G>C	GRCh37
NC_000005.8:g.131750573G>C	NCBI36
NG_008982.1:g.22274G>C
NG_008982.2:g.22279G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.666-43G>C	ENSP00000388838.2:n.666-43G>C
ENST00000435065.7:c.897-43G>C	ENSP00000402760.2:n.897-43G>C
ENST00000448810.6:c.825-43G>C	ENSP00000401860.2:n.825-43G>C
ENST00000686757.1:c.844-43G>C	ENSP00000510721.1:n.844-43G>C
ENST00000687740.1:n.3467G>C
ENST00000688151.1:n.2135-43G>C
ENST00000689271.1:c.672-43G>C	ENSP00000510797.1:n.672-43G>C
ENST00000690900.1:c.796-43G>C	ENSP00000510703.1:n.796-43G>C
ENST00000692212.1:n.769-43G>C
ENST00000692355.1:c.205-1939G>C
ENST00000692413.1:c.844-80G>C	ENSP00000509374.1:n.844-80G>C
ENST00000692825.1:c.893-43G>C	ENSP00000509447.1:n.893-43G>C
ENST00000693308.1:c.838-8G>C	ENSP00000509770.1:n.838-8G>C
ENST00000693763.1:n.1985-43G>C
ENST00000245407.8:c.825-43G>C MANE Select	ENSP00000245407.3:n.825-43G>C
ENST00000245407.7:c.825-43G>C	ENSP00000245407.3:n.825-43G>C
ENST00000415928.5:c.594-43G>C	ENSP00000388838.1:n.594-43G>C
ENST00000435065.6:c.897-43G>C	ENSP00000402760.2:n.897-43G>C
ENST00000437841.6:c.*140-43G>C	ENSP00000400553.1:n.*140-43G>C
ENST00000448810.5:c.173-43G>C
ENST00000461013.5:n.8247-43G>C
NM_001308122.1:c.897-43G>C	NP_001295051.1:n.897-43G>C
NM_003060.3:c.825-43G>C	NP_003051.1:n.825-43G>C
XM_011543590.1:c.207-43G>C	XP_011541892.1:n.207-43G>C
XR_427718.1:n.1185-43G>C
XR_948290.1:n.1166-43G>C
XR_948291.1:n.1179-43G>C
XM_011543590.2:c.207-43G>C	XP_011541892.1:n.207-43G>C
XM_017009778.2:c.297-43G>C	XP_016865267.1:n.297-43G>C
XR_001742215.1:n.1166-43G>C
XR_001742216.1:n.1185-43G>C
XR_427718.2:n.1185-43G>C
XR_948290.2:n.1166-43G>C
XR_948291.2:n.1179-43G>C
NM_003060.4:c.825-43G>C MANE Select	NP_003051.1:n.825-43G>C
NM_001308122.2:c.897-43G>C	NP_001295051.1:n.897-43G>C