Canonical Allele Identifier: CA360804541

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131719853A>C (hg19) ; chr5:g.132384161A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384161A>C , CM000667.2:g.132384161A>C	GRCh38
NC_000005.9:g.131719853A>C , CM000667.1:g.131719853A>C	GRCh37
NC_000005.8:g.131747752A>C	NCBI36
NG_008982.1:g.19453A>C
NG_008982.2:g.19458A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.512A>C	ENSP00000388838.2:p.Asn171Thr
ENST00000435065.7:c.584A>C	ENSP00000402760.2:p.Asn195Thr
ENST00000448810.6:c.512A>C	ENSP00000401860.2:p.Asn171Thr
ENST00000686757.1:c.512A>C	ENSP00000510721.1:p.Asn171Thr
ENST00000687740.1:n.646A>C
ENST00000688151.1:n.1691A>C
ENST00000689271.1:c.512A>C	ENSP00000510797.1:p.Asn171Thr
ENST00000690900.1:c.512A>C	ENSP00000510703.1:p.Asn171Thr
ENST00000692355.1:c.64A>C
ENST00000692413.1:c.512A>C	ENSP00000509374.1:p.Asn171Thr
ENST00000692825.1:c.580A>C	ENSP00000509447.1:n.580A>C
ENST00000693308.1:c.512A>C	ENSP00000509770.1:p.Asn171Thr
ENST00000693763.1:n.646A>C
ENST00000245407.8:c.512A>C MANE Select	ENSP00000245407.3:p.Asn171Thr
ENST00000245407.7:c.512A>C	ENSP00000245407.3:p.Asn171Thr
ENST00000415928.5:c.281A>C	ENSP00000388838.1:p.Asn94Thr
ENST00000435065.6:c.584A>C	ENSP00000402760.2:p.Asn195Thr
ENST00000437841.6:c.394-1167A>C	ENSP00000400553.1:n.394-1167A>C
ENST00000461013.5:n.7934A>C
NM_001308122.1:c.584A>C	NP_001295051.1:p.Asn195Thr
NM_003060.3:c.512A>C	NP_003051.1:p.Asn171Thr
XR_427718.1:n.853A>C
XR_948290.1:n.853A>C
XR_948291.1:n.853A>C
XM_011543590.2:c.-120A>C	XP_011541892.1:n.-120A>C
XM_017009778.2:c.-17A>C	XP_016865267.1:n.-17A>C
XR_001742215.1:n.853A>C
XR_001742216.1:n.853A>C
XR_427718.2:n.853A>C
XR_948290.2:n.853A>C
XR_948291.2:n.853A>C
NM_003060.4:c.512A>C MANE Select	NP_003051.1:p.Asn171Thr
NM_001308122.2:c.584A>C	NP_001295051.1:p.Asn195Thr