Canonical Allele Identifier: CA446337606

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726415G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390723G>C , CM000667.2:g.132390723G>C	GRCh38
NC_000005.9:g.131726415G>C , CM000667.1:g.131726415G>C	GRCh37
NC_000005.8:g.131754314G>C	NCBI36
NG_008982.1:g.26015G>C
NG_008982.2:g.26020G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.927G>C	ENSP00000388838.2:p.Ser309=
ENST00000435065.7:c.1158G>C	ENSP00000402760.2:p.Ser386=
ENST00000448810.6:c.1053-53G>C	ENSP00000401860.2:n.1053-53G>C
ENST00000685543.1:n.1227G>C
ENST00000686757.1:c.*250G>C	ENSP00000510721.1:n.*250G>C
ENST00000687740.1:n.3771G>C
ENST00000688151.1:n.2396G>C
ENST00000689271.1:c.933G>C	ENSP00000510797.1:p.Ser311=
ENST00000690900.1:c.*250G>C	ENSP00000510703.1:n.*250G>C
ENST00000692212.1:n.2698G>C
ENST00000692355.1:c.339G>C
ENST00000692413.1:c.1068G>C	ENSP00000509374.1:p.Ser356=
ENST00000692825.1:c.1154G>C	ENSP00000509447.1:n.1154G>C
ENST00000693308.1:c.1134G>C	ENSP00000509770.1:p.Ser378=
ENST00000693763.1:n.2246G>C
ENST00000245407.8:c.1086G>C MANE Select	ENSP00000245407.3:p.Ser362=
ENST00000245407.7:c.1086G>C	ENSP00000245407.3:p.Ser362=
ENST00000435065.6:c.1158G>C	ENSP00000402760.2:p.Ser386=
ENST00000447841.5:c.111+1702G>C
ENST00000448810.5:c.401-53G>C
ENST00000461013.5:n.8508G>C
ENST00000475308.1:n.1764G>C
ENST00000479605.5:n.189G>C
NM_001308122.1:c.1158G>C	NP_001295051.1:p.Ser386=
NM_003060.3:c.1086G>C	NP_003051.1:p.Ser362=
XM_011543590.1:c.468G>C	XP_011541892.1:p.Ser156=
XR_427718.1:n.1446G>C
XR_948290.1:n.1393+1702G>C
XR_948291.1:n.1440G>C
XM_011543590.2:c.468G>C	XP_011541892.1:p.Ser156=
XM_017009778.2:c.558G>C	XP_016865267.1:p.Ser186=
XR_001742215.1:n.1394-53G>C
XR_001742216.1:n.1413-53G>C
XR_427718.2:n.1446G>C
XR_948290.2:n.1393+1702G>C
XR_948291.2:n.1440G>C
NM_003060.4:c.1086G>C MANE Select	NP_003051.1:p.Ser362=
NM_001308122.2:c.1158G>C	NP_001295051.1:p.Ser386=