Canonical Allele Identifier: CA360805226

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721162G>C (hg19) ; chr5:g.132385470G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385470G>C , CM000667.2:g.132385470G>C	GRCh38
NC_000005.9:g.131721162G>C , CM000667.1:g.131721162G>C	GRCh37
NC_000005.8:g.131749061G>C	NCBI36
NG_008982.1:g.20762G>C
NG_008982.2:g.20767G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1156G>C	ENSP00000388838.2:n.665+1156G>C
ENST00000435065.7:c.867G>C	ENSP00000402760.2:p.Met289Ile
ENST00000448810.6:c.795G>C	ENSP00000401860.2:p.Met265Ile
ENST00000686757.1:c.814G>C	ENSP00000510721.1:p.Ala272Pro
ENST00000687740.1:n.1955G>C
ENST00000688151.1:n.1987G>C
ENST00000689271.1:c.671+1150G>C	ENSP00000510797.1:n.671+1150G>C
ENST00000690900.1:c.766G>C	ENSP00000510703.1:p.Ala256Pro
ENST00000692212.1:n.621G>C
ENST00000692355.1:c.204+1169G>C
ENST00000692413.1:c.814G>C	ENSP00000509374.1:p.Ala272Pro
ENST00000692825.1:c.863G>C	ENSP00000509447.1:n.863G>C
ENST00000693308.1:c.808G>C	ENSP00000509770.1:p.Ala270Pro
ENST00000693763.1:n.1955G>C
ENST00000245407.8:c.795G>C MANE Select	ENSP00000245407.3:p.Met265Ile
ENST00000245407.7:c.795G>C	ENSP00000245407.3:p.Met265Ile
ENST00000415928.5:c.564G>C	ENSP00000388838.1:p.Met188Ile
ENST00000435065.6:c.867G>C	ENSP00000402760.2:p.Met289Ile
ENST00000437841.6:c.*110G>C	ENSP00000400553.1:n.*110G>C
ENST00000448810.5:c.143G>C
ENST00000461013.5:n.8217G>C
NM_001308122.1:c.867G>C	NP_001295051.1:p.Met289Ile
NM_003060.3:c.795G>C	NP_003051.1:p.Met265Ile
XM_011543590.1:c.177G>C	XP_011541892.1:p.Met59Ile
XR_427718.1:n.1155G>C
XR_948290.1:n.1136G>C
XR_948291.1:n.1149G>C
XM_011543590.2:c.177G>C	XP_011541892.1:p.Met59Ile
XM_017009778.2:c.267G>C	XP_016865267.1:p.Met89Ile
XR_001742215.1:n.1136G>C
XR_001742216.1:n.1155G>C
XR_427718.2:n.1155G>C
XR_948290.2:n.1136G>C
XR_948291.2:n.1149G>C
NM_003060.4:c.795G>C MANE Select	NP_003051.1:p.Met265Ile
NM_001308122.2:c.867G>C	NP_001295051.1:p.Met289Ile