Canonical Allele Identifier: CA360804986

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721043G>C (hg19) ; chr5:g.132385351G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385351G>C , CM000667.2:g.132385351G>C	GRCh38
NC_000005.9:g.131721043G>C , CM000667.1:g.131721043G>C	GRCh37
NC_000005.8:g.131748942G>C	NCBI36
NG_008982.1:g.20643G>C
NG_008982.2:g.20648G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1037G>C	ENSP00000388838.2:n.665+1037G>C
ENST00000435065.7:c.748G>C	ENSP00000402760.2:p.Val250Leu
ENST00000448810.6:c.676G>C	ENSP00000401860.2:p.Val226Leu
ENST00000686757.1:c.695G>C	ENSP00000510721.1:p.Ser232Thr
ENST00000687740.1:n.1836G>C
ENST00000688151.1:n.1868G>C
ENST00000689271.1:c.671+1031G>C	ENSP00000510797.1:n.671+1031G>C
ENST00000690900.1:c.672-25G>C	ENSP00000510703.1:n.672-25G>C
ENST00000692212.1:n.502G>C
ENST00000692355.1:c.204+1050G>C
ENST00000692413.1:c.695G>C	ENSP00000509374.1:p.Ser232Thr
ENST00000692825.1:c.744G>C	ENSP00000509447.1:n.744G>C
ENST00000693308.1:c.689G>C	ENSP00000509770.1:p.Ser230Thr
ENST00000693763.1:n.1836G>C
ENST00000245407.8:c.676G>C MANE Select	ENSP00000245407.3:p.Val226Leu
ENST00000245407.7:c.676G>C	ENSP00000245407.3:p.Val226Leu
ENST00000415928.5:c.445G>C	ENSP00000388838.1:p.Val149Leu
ENST00000435065.6:c.748G>C	ENSP00000402760.2:p.Val250Leu
ENST00000437841.6:c.417G>C	ENSP00000400553.1:p.Gln139His
ENST00000448810.5:c.24G>C
ENST00000461013.5:n.8098G>C
NM_001308122.1:c.748G>C	NP_001295051.1:p.Val250Leu
NM_003060.3:c.676G>C	NP_003051.1:p.Val226Leu
XM_011543590.1:c.58G>C	XP_011541892.1:p.Val20Leu
XR_427718.1:n.1036G>C
XR_948290.1:n.1017G>C
XR_948291.1:n.1030G>C
XM_011543590.2:c.58G>C	XP_011541892.1:p.Val20Leu
XM_017009778.2:c.148G>C	XP_016865267.1:p.Val50Leu
XR_001742215.1:n.1017G>C
XR_001742216.1:n.1036G>C
XR_427718.2:n.1036G>C
XR_948290.2:n.1017G>C
XR_948291.2:n.1030G>C
NM_003060.4:c.676G>C MANE Select	NP_003051.1:p.Val226Leu
NM_001308122.2:c.748G>C	NP_001295051.1:p.Val250Leu