Canonical Allele Identifier: CA360804610

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131719871T>G (hg19) ; chr5:g.132384179T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384179T>G , CM000667.2:g.132384179T>G	GRCh38
NC_000005.9:g.131719871T>G , CM000667.1:g.131719871T>G	GRCh37
NC_000005.8:g.131747770T>G	NCBI36
NG_008982.1:g.19471T>G
NG_008982.2:g.19476T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.530T>G	ENSP00000388838.2:p.Met177Arg
ENST00000435065.7:c.602T>G	ENSP00000402760.2:p.Met201Arg
ENST00000448810.6:c.530T>G	ENSP00000401860.2:p.Met177Arg
ENST00000686757.1:c.530T>G	ENSP00000510721.1:p.Met177Arg
ENST00000687740.1:n.664T>G
ENST00000688151.1:n.1709T>G
ENST00000689271.1:c.530T>G	ENSP00000510797.1:p.Met177Arg
ENST00000690900.1:c.530T>G	ENSP00000510703.1:p.Met177Arg
ENST00000692355.1:c.82T>G
ENST00000692413.1:c.530T>G	ENSP00000509374.1:p.Met177Arg
ENST00000692825.1:c.598T>G	ENSP00000509447.1:n.598T>G
ENST00000693308.1:c.530T>G	ENSP00000509770.1:p.Met177Arg
ENST00000693763.1:n.664T>G
ENST00000245407.8:c.530T>G MANE Select	ENSP00000245407.3:p.Met177Arg
ENST00000245407.7:c.530T>G	ENSP00000245407.3:p.Met177Arg
ENST00000415928.5:c.299T>G	ENSP00000388838.1:p.Met100Arg
ENST00000435065.6:c.602T>G	ENSP00000402760.2:p.Met201Arg
ENST00000437841.6:c.394-1149T>G	ENSP00000400553.1:n.394-1149T>G
ENST00000461013.5:n.7952T>G
NM_001308122.1:c.602T>G	NP_001295051.1:p.Met201Arg
NM_003060.3:c.530T>G	NP_003051.1:p.Met177Arg
XR_427718.1:n.871T>G
XR_948290.1:n.871T>G
XR_948291.1:n.871T>G
XM_011543590.2:c.-102T>G	XP_011541892.1:n.-102T>G
XM_017009778.2:c.2T>G	XP_016865267.1:p.Met1Arg
XR_001742215.1:n.871T>G
XR_001742216.1:n.871T>G
XR_427718.2:n.871T>G
XR_948290.2:n.871T>G
XR_948291.2:n.871T>G
NM_003060.4:c.530T>G MANE Select	NP_003051.1:p.Met177Arg
NM_001308122.2:c.602T>G	NP_001295051.1:p.Met201Arg