Canonical Allele Identifier: CA360805223

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721161T>C (hg19) ; chr5:g.132385469T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385469T>C , CM000667.2:g.132385469T>C	GRCh38
NC_000005.9:g.131721161T>C , CM000667.1:g.131721161T>C	GRCh37
NC_000005.8:g.131749060T>C	NCBI36
NG_008982.1:g.20761T>C
NG_008982.2:g.20766T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1155T>C	ENSP00000388838.2:n.665+1155T>C
ENST00000435065.7:c.866T>C	ENSP00000402760.2:p.Met289Thr
ENST00000448810.6:c.794T>C	ENSP00000401860.2:p.Met265Thr
ENST00000686757.1:c.813T>C	ENSP00000510721.1:p.Asp271=
ENST00000687740.1:n.1954T>C
ENST00000688151.1:n.1986T>C
ENST00000689271.1:c.671+1149T>C	ENSP00000510797.1:n.671+1149T>C
ENST00000690900.1:c.765T>C	ENSP00000510703.1:p.Asp255=
ENST00000692212.1:n.620T>C
ENST00000692355.1:c.204+1168T>C
ENST00000692413.1:c.813T>C	ENSP00000509374.1:p.Asp271=
ENST00000692825.1:c.862T>C	ENSP00000509447.1:n.862T>C
ENST00000693308.1:c.807T>C	ENSP00000509770.1:p.Asp269=
ENST00000693763.1:n.1954T>C
ENST00000245407.8:c.794T>C MANE Select	ENSP00000245407.3:p.Met265Thr
ENST00000245407.7:c.794T>C	ENSP00000245407.3:p.Met265Thr
ENST00000415928.5:c.563T>C	ENSP00000388838.1:p.Met188Thr
ENST00000435065.6:c.866T>C	ENSP00000402760.2:p.Met289Thr
ENST00000437841.6:c.*109T>C	ENSP00000400553.1:n.*109T>C
ENST00000448810.5:c.142T>C
ENST00000461013.5:n.8216T>C
NM_001308122.1:c.866T>C	NP_001295051.1:p.Met289Thr
NM_003060.3:c.794T>C	NP_003051.1:p.Met265Thr
XM_011543590.1:c.176T>C	XP_011541892.1:p.Met59Thr
XR_427718.1:n.1154T>C
XR_948290.1:n.1135T>C
XR_948291.1:n.1148T>C
XM_011543590.2:c.176T>C	XP_011541892.1:p.Met59Thr
XM_017009778.2:c.266T>C	XP_016865267.1:p.Met89Thr
XR_001742215.1:n.1135T>C
XR_001742216.1:n.1154T>C
XR_427718.2:n.1154T>C
XR_948290.2:n.1135T>C
XR_948291.2:n.1148T>C
NM_003060.4:c.794T>C MANE Select	NP_003051.1:p.Met265Thr
NM_001308122.2:c.866T>C	NP_001295051.1:p.Met289Thr