Canonical Allele Identifier: CA446343171

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131728207A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392515A>C , CM000667.2:g.132392515A>C	GRCh38
NC_000005.9:g.131728207A>C , CM000667.1:g.131728207A>C	GRCh37
NC_000005.8:g.131756106A>C	NCBI36
NG_008982.1:g.27807A>C
NG_008982.2:g.27812A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1191A>C	ENSP00000388838.2:p.Thr397=
ENST00000435065.7:c.1422A>C	ENSP00000402760.2:p.Thr474=
ENST00000448810.6:c.*202A>C	ENSP00000401860.2:n.*202A>C
ENST00000685543.1:n.1491A>C
ENST00000686757.1:c.*514A>C	ENSP00000510721.1:n.*514A>C
ENST00000687740.1:n.4035A>C
ENST00000688151.1:n.2660A>C
ENST00000689271.1:c.1197A>C	ENSP00000510797.1:p.Thr399=
ENST00000690900.1:c.*514A>C	ENSP00000510703.1:n.*514A>C
ENST00000692212.1:n.4490A>C
ENST00000692355.1:c.603A>C
ENST00000692413.1:c.1332A>C	ENSP00000509374.1:p.Thr444=
ENST00000692825.1:c.1418A>C	ENSP00000509447.1:n.1418A>C
ENST00000693308.1:c.1398A>C	ENSP00000509770.1:p.Thr466=
ENST00000693763.1:n.2510A>C
ENST00000245407.8:c.1350A>C MANE Select	ENSP00000245407.3:p.Thr450=
ENST00000245407.7:c.1350A>C	ENSP00000245407.3:p.Thr450=
ENST00000435065.6:c.1422A>C	ENSP00000402760.2:p.Thr474=
ENST00000447841.5:c.194A>C
ENST00000448810.5:c.612A>C
ENST00000461013.5:n.8772A>C
ENST00000475308.1:n.2028A>C
ENST00000479605.5:n.453A>C
NM_001308122.1:c.1422A>C	NP_001295051.1:p.Thr474=
NM_003060.3:c.1350A>C	NP_003051.1:p.Thr450=
XM_011543590.1:c.732A>C	XP_011541892.1:p.Thr244=
XR_948290.1:n.1476A>C
XM_011543590.2:c.732A>C	XP_011541892.1:p.Thr244=
XM_017009778.2:c.822A>C	XP_016865267.1:p.Thr274=
XR_001742215.1:n.1605A>C
XR_001742216.1:n.1624A>C
XR_427718.2:n.1710A>C
XR_948290.2:n.1476A>C
XR_948291.2:n.1704A>C
NM_003060.4:c.1350A>C MANE Select	NP_003051.1:p.Thr450=
NM_001308122.2:c.1422A>C	NP_001295051.1:p.Thr474=