Canonical Allele Identifier: CA446329628

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131719857G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384165G>C , CM000667.2:g.132384165G>C	GRCh38
NC_000005.9:g.131719857G>C , CM000667.1:g.131719857G>C	GRCh37
NC_000005.8:g.131747756G>C	NCBI36
NG_008982.1:g.19457G>C
NG_008982.2:g.19462G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.516G>C	ENSP00000388838.2:p.Val172=
ENST00000435065.7:c.588G>C	ENSP00000402760.2:p.Val196=
ENST00000448810.6:c.516G>C	ENSP00000401860.2:p.Val172=
ENST00000686757.1:c.516G>C	ENSP00000510721.1:p.Val172=
ENST00000687740.1:n.650G>C
ENST00000688151.1:n.1695G>C
ENST00000689271.1:c.516G>C	ENSP00000510797.1:p.Val172=
ENST00000690900.1:c.516G>C	ENSP00000510703.1:p.Val172=
ENST00000692355.1:c.68G>C
ENST00000692413.1:c.516G>C	ENSP00000509374.1:p.Val172=
ENST00000692825.1:c.584G>C	ENSP00000509447.1:n.584G>C
ENST00000693308.1:c.516G>C	ENSP00000509770.1:p.Val172=
ENST00000693763.1:n.650G>C
ENST00000245407.8:c.516G>C MANE Select	ENSP00000245407.3:p.Val172=
ENST00000245407.7:c.516G>C	ENSP00000245407.3:p.Val172=
ENST00000415928.5:c.285G>C	ENSP00000388838.1:p.Val95=
ENST00000435065.6:c.588G>C	ENSP00000402760.2:p.Val196=
ENST00000437841.6:c.394-1163G>C	ENSP00000400553.1:n.394-1163G>C
ENST00000461013.5:n.7938G>C
NM_001308122.1:c.588G>C	NP_001295051.1:p.Val196=
NM_003060.3:c.516G>C	NP_003051.1:p.Val172=
XR_427718.1:n.857G>C
XR_948290.1:n.857G>C
XR_948291.1:n.857G>C
XM_011543590.2:c.-116G>C	XP_011541892.1:n.-116G>C
XM_017009778.2:c.-13G>C	XP_016865267.1:n.-13G>C
XR_001742215.1:n.857G>C
XR_001742216.1:n.857G>C
XR_427718.2:n.857G>C
XR_948290.2:n.857G>C
XR_948291.2:n.857G>C
NM_003060.4:c.516G>C MANE Select	NP_003051.1:p.Val172=
NM_001308122.2:c.588G>C	NP_001295051.1:p.Val196=