Canonical Allele Identifier: CA446332416

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131722723C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387031C>A , CM000667.2:g.132387031C>A	GRCh38
NC_000005.9:g.131722723C>A , CM000667.1:g.131722723C>A	GRCh37
NC_000005.8:g.131750622C>A	NCBI36
NG_008982.1:g.22323C>A
NG_008982.2:g.22328C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.672C>A	ENSP00000388838.2:p.Ile224=
ENST00000435065.7:c.903C>A	ENSP00000402760.2:p.Ile301=
ENST00000448810.6:c.831C>A	ENSP00000401860.2:p.Ile277=
ENST00000686757.1:c.850C>A	ENSP00000510721.1:p.Pro284Thr
ENST00000687740.1:n.3516C>A
ENST00000688151.1:n.2141C>A
ENST00000689271.1:c.678C>A	ENSP00000510797.1:p.Ile226=
ENST00000690900.1:c.802C>A	ENSP00000510703.1:p.Pro268Thr
ENST00000692212.1:n.775C>A
ENST00000692355.1:c.205-1890C>A
ENST00000692413.1:c.844-31C>A	ENSP00000509374.1:n.844-31C>A
ENST00000692825.1:c.899C>A	ENSP00000509447.1:n.899C>A
ENST00000693308.1:c.879C>A	ENSP00000509770.1:p.Ile293=
ENST00000693763.1:n.1991C>A
ENST00000245407.8:c.831C>A MANE Select	ENSP00000245407.3:p.Ile277=
ENST00000245407.7:c.831C>A	ENSP00000245407.3:p.Ile277=
ENST00000415928.5:c.600C>A	ENSP00000388838.1:p.Ile200=
ENST00000435065.6:c.903C>A	ENSP00000402760.2:p.Ile301=
ENST00000437841.6:c.*146C>A	ENSP00000400553.1:n.*146C>A
ENST00000448810.5:c.179C>A
ENST00000461013.5:n.8253C>A
NM_001308122.1:c.903C>A	NP_001295051.1:p.Ile301=
NM_003060.3:c.831C>A	NP_003051.1:p.Ile277=
XM_011543590.1:c.213C>A	XP_011541892.1:p.Ile71=
XR_427718.1:n.1191C>A
XR_948290.1:n.1172C>A
XR_948291.1:n.1185C>A
XM_011543590.2:c.213C>A	XP_011541892.1:p.Ile71=
XM_017009778.2:c.303C>A	XP_016865267.1:p.Ile101=
XR_001742215.1:n.1172C>A
XR_001742216.1:n.1191C>A
XR_427718.2:n.1191C>A
XR_948290.2:n.1172C>A
XR_948291.2:n.1185C>A
NM_003060.4:c.831C>A MANE Select	NP_003051.1:p.Ile277=
NM_001308122.2:c.903C>A	NP_001295051.1:p.Ile301=