Canonical Allele Identifier: CA360805241

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131721172C>G (hg19) ; chr5:g.132385480C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385480C>G , CM000667.2:g.132385480C>G	GRCh38
NC_000005.9:g.131721172C>G , CM000667.1:g.131721172C>G	GRCh37
NC_000005.8:g.131749071C>G	NCBI36
NG_008982.1:g.20772C>G
NG_008982.2:g.20777C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+1166C>G	ENSP00000388838.2:n.665+1166C>G
ENST00000435065.7:c.877C>G	ENSP00000402760.2:p.Leu293Val
ENST00000448810.6:c.805C>G	ENSP00000401860.2:p.Leu269Val
ENST00000686757.1:c.824C>G	ENSP00000510721.1:p.Ala275Gly
ENST00000687740.1:n.1965C>G
ENST00000688151.1:n.1997C>G
ENST00000689271.1:c.671+1160C>G	ENSP00000510797.1:n.671+1160C>G
ENST00000690900.1:c.776C>G	ENSP00000510703.1:p.Ala259Gly
ENST00000692212.1:n.631C>G
ENST00000692355.1:c.204+1179C>G
ENST00000692413.1:c.824C>G	ENSP00000509374.1:p.Ala275Gly
ENST00000692825.1:c.873C>G	ENSP00000509447.1:n.873C>G
ENST00000693308.1:c.818C>G	ENSP00000509770.1:p.Ala273Gly
ENST00000693763.1:n.1965C>G
ENST00000245407.8:c.805C>G MANE Select	ENSP00000245407.3:p.Leu269Val
ENST00000245407.7:c.805C>G	ENSP00000245407.3:p.Leu269Val
ENST00000415928.5:c.574C>G	ENSP00000388838.1:p.Leu192Val
ENST00000435065.6:c.877C>G	ENSP00000402760.2:p.Leu293Val
ENST00000437841.6:c.*120C>G	ENSP00000400553.1:n.*120C>G
ENST00000448810.5:c.153C>G
ENST00000461013.5:n.8227C>G
NM_001308122.1:c.877C>G	NP_001295051.1:p.Leu293Val
NM_003060.3:c.805C>G	NP_003051.1:p.Leu269Val
XM_011543590.1:c.187C>G	XP_011541892.1:p.Leu63Val
XR_427718.1:n.1165C>G
XR_948290.1:n.1146C>G
XR_948291.1:n.1159C>G
XM_011543590.2:c.187C>G	XP_011541892.1:p.Leu63Val
XM_017009778.2:c.277C>G	XP_016865267.1:p.Leu93Val
XR_001742215.1:n.1146C>G
XR_001742216.1:n.1165C>G
XR_427718.2:n.1165C>G
XR_948290.2:n.1146C>G
XR_948291.2:n.1159C>G
NM_003060.4:c.805C>G MANE Select	NP_003051.1:p.Leu269Val
NM_001308122.2:c.877C>G	NP_001295051.1:p.Leu293Val