Canonical Allele Identifier: CA360805075

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721089T>A (hg19) ; chr5:g.132385397T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385397T>A , CM000667.2:g.132385397T>A	GRCh38
NC_000005.9:g.131721089T>A , CM000667.1:g.131721089T>A	GRCh37
NC_000005.8:g.131748988T>A	NCBI36
NG_008982.1:g.20689T>A
NG_008982.2:g.20694T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1083T>A	ENSP00000388838.2:n.665+1083T>A
ENST00000435065.7:c.794T>A	ENSP00000402760.2:p.Phe265Tyr
ENST00000448810.6:c.722T>A	ENSP00000401860.2:p.Phe241Tyr
ENST00000686757.1:c.741T>A	ENSP00000510721.1:p.Ile247=
ENST00000687740.1:n.1882T>A
ENST00000688151.1:n.1914T>A
ENST00000689271.1:c.671+1077T>A	ENSP00000510797.1:n.671+1077T>A
ENST00000690900.1:c.693T>A	ENSP00000510703.1:p.Ile231=
ENST00000692212.1:n.548T>A
ENST00000692355.1:c.204+1096T>A
ENST00000692413.1:c.741T>A	ENSP00000509374.1:p.Ile247=
ENST00000692825.1:c.790T>A	ENSP00000509447.1:n.790T>A
ENST00000693308.1:c.735T>A	ENSP00000509770.1:p.Ile245=
ENST00000693763.1:n.1882T>A
ENST00000245407.8:c.722T>A MANE Select	ENSP00000245407.3:p.Phe241Tyr
ENST00000245407.7:c.722T>A	ENSP00000245407.3:p.Phe241Tyr
ENST00000415928.5:c.491T>A	ENSP00000388838.1:p.Phe164Tyr
ENST00000435065.6:c.794T>A	ENSP00000402760.2:p.Phe265Tyr
ENST00000437841.6:c.*37T>A	ENSP00000400553.1:n.*37T>A
ENST00000448810.5:c.70T>A
ENST00000461013.5:n.8144T>A
NM_001308122.1:c.794T>A	NP_001295051.1:p.Phe265Tyr
NM_003060.3:c.722T>A	NP_003051.1:p.Phe241Tyr
XM_011543590.1:c.104T>A	XP_011541892.1:p.Phe35Tyr
XR_427718.1:n.1082T>A
XR_948290.1:n.1063T>A
XR_948291.1:n.1076T>A
XM_011543590.2:c.104T>A	XP_011541892.1:p.Phe35Tyr
XM_017009778.2:c.194T>A	XP_016865267.1:p.Phe65Tyr
XR_001742215.1:n.1063T>A
XR_001742216.1:n.1082T>A
XR_427718.2:n.1082T>A
XR_948290.2:n.1063T>A
XR_948291.2:n.1076T>A
NM_003060.4:c.722T>A MANE Select	NP_003051.1:p.Phe241Tyr
NM_001308122.2:c.794T>A	NP_001295051.1:p.Phe265Tyr