Canonical Allele Identifier: CA2675200459

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132385543-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385543T>C , CM000667.2:g.132385543T>C	GRCh38
NC_000005.9:g.131721235T>C , CM000667.1:g.131721235T>C	GRCh37
NC_000005.8:g.131749134T>C	NCBI36
NG_008982.1:g.20835T>C
NG_008982.2:g.20840T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1229T>C	ENSP00000388838.2:n.665+1229T>C
ENST00000435065.7:c.896+44T>C	ENSP00000402760.2:n.896+44T>C
ENST00000448810.6:c.824+44T>C	ENSP00000401860.2:n.824+44T>C
ENST00000686757.1:c.843+44T>C	ENSP00000510721.1:n.843+44T>C
ENST00000687740.1:n.2028T>C
ENST00000688151.1:n.2016+44T>C
ENST00000689271.1:c.671+1223T>C	ENSP00000510797.1:n.671+1223T>C
ENST00000690900.1:c.795+44T>C	ENSP00000510703.1:n.795+44T>C
ENST00000692212.1:n.650+44T>C
ENST00000692355.1:c.204+1242T>C
ENST00000692413.1:c.843+44T>C	ENSP00000509374.1:n.843+44T>C
ENST00000692825.1:c.892+44T>C	ENSP00000509447.1:n.892+44T>C
ENST00000693308.1:c.837+44T>C	ENSP00000509770.1:n.837+44T>C
ENST00000693763.1:n.1984+44T>C
ENST00000245407.8:c.824+44T>C MANE Select	ENSP00000245407.3:n.824+44T>C
ENST00000245407.7:c.824+44T>C	ENSP00000245407.3:n.824+44T>C
ENST00000415928.5:c.593+44T>C	ENSP00000388838.1:n.593+44T>C
ENST00000435065.6:c.896+44T>C	ENSP00000402760.2:n.896+44T>C
ENST00000437841.6:c.*139+44T>C	ENSP00000400553.1:n.*139+44T>C
ENST00000448810.5:c.172+44T>C
ENST00000461013.5:n.8246+44T>C
NM_001308122.1:c.896+44T>C	NP_001295051.1:n.896+44T>C
NM_003060.3:c.824+44T>C	NP_003051.1:n.824+44T>C
XM_011543590.1:c.206+44T>C	XP_011541892.1:n.206+44T>C
XR_427718.1:n.1184+44T>C
XR_948290.1:n.1165+44T>C
XR_948291.1:n.1178+44T>C
XM_011543590.2:c.206+44T>C	XP_011541892.1:n.206+44T>C
XM_017009778.2:c.296+44T>C	XP_016865267.1:n.296+44T>C
XR_001742215.1:n.1165+44T>C
XR_001742216.1:n.1184+44T>C
XR_427718.2:n.1184+44T>C
XR_948290.2:n.1165+44T>C
XR_948291.2:n.1178+44T>C
NM_003060.4:c.824+44T>C MANE Select	NP_003051.1:n.824+44T>C
NM_001308122.2:c.896+44T>C	NP_001295051.1:n.896+44T>C