Canonical Allele Identifier: CA360807800

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726564G>C (hg19) ; chr5:g.132390872G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390872G>C , CM000667.2:g.132390872G>C	GRCh38
NC_000005.9:g.131726564G>C , CM000667.1:g.131726564G>C	GRCh37
NC_000005.8:g.131754463G>C	NCBI36
NG_008982.1:g.26164G>C
NG_008982.2:g.26169G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1076G>C	ENSP00000388838.2:p.Ser359Thr
ENST00000435065.7:c.1307G>C	ENSP00000402760.2:p.Ser436Thr
ENST00000448810.6:c.*87G>C	ENSP00000401860.2:n.*87G>C
ENST00000685543.1:n.1376G>C
ENST00000686757.1:c.*399G>C	ENSP00000510721.1:n.*399G>C
ENST00000687740.1:n.3920G>C
ENST00000688151.1:n.2545G>C
ENST00000689271.1:c.1082G>C	ENSP00000510797.1:p.Ser361Thr
ENST00000690900.1:c.*399G>C	ENSP00000510703.1:n.*399G>C
ENST00000692212.1:n.2847G>C
ENST00000692355.1:c.488G>C
ENST00000692413.1:c.1217G>C	ENSP00000509374.1:p.Ser406Thr
ENST00000692825.1:c.1303G>C	ENSP00000509447.1:n.1303G>C
ENST00000693308.1:c.1283G>C	ENSP00000509770.1:p.Ser428Thr
ENST00000693763.1:n.2395G>C
ENST00000245407.8:c.1235G>C MANE Select	ENSP00000245407.3:p.Ser412Thr
ENST00000245407.7:c.1235G>C	ENSP00000245407.3:p.Ser412Thr
ENST00000435065.6:c.1307G>C	ENSP00000402760.2:p.Ser436Thr
ENST00000447841.5:c.112-1561G>C
ENST00000448810.5:c.497G>C
ENST00000461013.5:n.8657G>C
ENST00000475308.1:n.1913G>C
ENST00000479605.5:n.338G>C
NM_001308122.1:c.1307G>C	NP_001295051.1:p.Ser436Thr
NM_003060.3:c.1235G>C	NP_003051.1:p.Ser412Thr
XM_011543590.1:c.617G>C	XP_011541892.1:p.Ser206Thr
XR_427718.1:n.1595G>C
XR_948290.1:n.1394-1561G>C
XR_948291.1:n.1589G>C
XM_011543590.2:c.617G>C	XP_011541892.1:p.Ser206Thr
XM_017009778.2:c.707G>C	XP_016865267.1:p.Ser236Thr
XR_001742215.1:n.1490G>C
XR_001742216.1:n.1509G>C
XR_427718.2:n.1595G>C
XR_948290.2:n.1394-1561G>C
XR_948291.2:n.1589G>C
NM_003060.4:c.1235G>C MANE Select	NP_003051.1:p.Ser412Thr
NM_001308122.2:c.1307G>C	NP_001295051.1:p.Ser436Thr