Canonical Allele Identifier: CA360804957

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721029T>C (hg19) ; chr5:g.132385337T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385337T>C , CM000667.2:g.132385337T>C	GRCh38
NC_000005.9:g.131721029T>C , CM000667.1:g.131721029T>C	GRCh37
NC_000005.8:g.131748928T>C	NCBI36
NG_008982.1:g.20629T>C
NG_008982.2:g.20634T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1023T>C	ENSP00000388838.2:n.665+1023T>C
ENST00000435065.7:c.734T>C	ENSP00000402760.2:p.Ile245Thr
ENST00000448810.6:c.662T>C	ENSP00000401860.2:p.Ile221Thr
ENST00000686757.1:c.681T>C	ENSP00000510721.1:p.Asn227=
ENST00000687740.1:n.1822T>C
ENST00000688151.1:n.1854T>C
ENST00000689271.1:c.671+1017T>C	ENSP00000510797.1:n.671+1017T>C
ENST00000690900.1:c.672-39T>C	ENSP00000510703.1:n.672-39T>C
ENST00000692212.1:n.488T>C
ENST00000692355.1:c.204+1036T>C
ENST00000692413.1:c.681T>C	ENSP00000509374.1:p.Asn227=
ENST00000692825.1:c.730T>C	ENSP00000509447.1:n.730T>C
ENST00000693308.1:c.675T>C	ENSP00000509770.1:p.Asn225=
ENST00000693763.1:n.1822T>C
ENST00000245407.8:c.662T>C MANE Select	ENSP00000245407.3:p.Ile221Thr
ENST00000245407.7:c.662T>C	ENSP00000245407.3:p.Ile221Thr
ENST00000415928.5:c.431T>C	ENSP00000388838.1:p.Ile144Thr
ENST00000435065.6:c.734T>C	ENSP00000402760.2:p.Ile245Thr
ENST00000437841.6:c.403T>C	ENSP00000400553.1:p.Phe135Leu
ENST00000448810.5:c.10T>C
ENST00000461013.5:n.8084T>C
NM_001308122.1:c.734T>C	NP_001295051.1:p.Ile245Thr
NM_003060.3:c.662T>C	NP_003051.1:p.Ile221Thr
XM_011543590.1:c.44T>C	XP_011541892.1:p.Ile15Thr
XR_427718.1:n.1022T>C
XR_948290.1:n.1003T>C
XR_948291.1:n.1016T>C
XM_011543590.2:c.44T>C	XP_011541892.1:p.Ile15Thr
XM_017009778.2:c.134T>C	XP_016865267.1:p.Ile45Thr
XR_001742215.1:n.1003T>C
XR_001742216.1:n.1022T>C
XR_427718.2:n.1022T>C
XR_948290.2:n.1003T>C
XR_948291.2:n.1016T>C
NM_003060.4:c.662T>C MANE Select	NP_003051.1:p.Ile221Thr
NM_001308122.2:c.734T>C	NP_001295051.1:p.Ile245Thr