Canonical Allele Identifier: CA446330153

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721069A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385377A>C , CM000667.2:g.132385377A>C	GRCh38
NC_000005.9:g.131721069A>C , CM000667.1:g.131721069A>C	GRCh37
NC_000005.8:g.131748968A>C	NCBI36
NG_008982.1:g.20669A>C
NG_008982.2:g.20674A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+1063A>C	ENSP00000388838.2:n.665+1063A>C
ENST00000435065.7:c.774A>C	ENSP00000402760.2:p.Gly258=
ENST00000448810.6:c.702A>C	ENSP00000401860.2:p.Gly234=
ENST00000686757.1:c.721A>C	ENSP00000510721.1:p.Ser241Arg
ENST00000687740.1:n.1862A>C
ENST00000688151.1:n.1894A>C
ENST00000689271.1:c.671+1057A>C	ENSP00000510797.1:n.671+1057A>C
ENST00000690900.1:c.673A>C	ENSP00000510703.1:p.Ser225Arg
ENST00000692212.1:n.528A>C
ENST00000692355.1:c.204+1076A>C
ENST00000692413.1:c.721A>C	ENSP00000509374.1:p.Ser241Arg
ENST00000692825.1:c.770A>C	ENSP00000509447.1:n.770A>C
ENST00000693308.1:c.715A>C	ENSP00000509770.1:p.Ser239Arg
ENST00000693763.1:n.1862A>C
ENST00000245407.8:c.702A>C MANE Select	ENSP00000245407.3:p.Gly234=
ENST00000245407.7:c.702A>C	ENSP00000245407.3:p.Gly234=
ENST00000415928.5:c.471A>C	ENSP00000388838.1:p.Gly157=
ENST00000435065.6:c.774A>C	ENSP00000402760.2:p.Gly258=
ENST00000437841.6:c.*17A>C	ENSP00000400553.1:n.*17A>C
ENST00000448810.5:c.50A>C
ENST00000461013.5:n.8124A>C
NM_001308122.1:c.774A>C	NP_001295051.1:p.Gly258=
NM_003060.3:c.702A>C	NP_003051.1:p.Gly234=
XM_011543590.1:c.84A>C	XP_011541892.1:p.Gly28=
XR_427718.1:n.1062A>C
XR_948290.1:n.1043A>C
XR_948291.1:n.1056A>C
XM_011543590.2:c.84A>C	XP_011541892.1:p.Gly28=
XM_017009778.2:c.174A>C	XP_016865267.1:p.Gly58=
XR_001742215.1:n.1043A>C
XR_001742216.1:n.1062A>C
XR_427718.2:n.1062A>C
XR_948290.2:n.1043A>C
XR_948291.2:n.1056A>C
NM_003060.4:c.702A>C MANE Select	NP_003051.1:p.Gly234=
NM_001308122.2:c.774A>C	NP_001295051.1:p.Gly258=