Canonical Allele Identifier: CA360809781

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729418C>A (hg19) ; chr5:g.132393726C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393726C>A , CM000667.2:g.132393726C>A	GRCh38
NC_000005.9:g.131729418C>A , CM000667.1:g.131729418C>A	GRCh37
NC_000005.8:g.131757317C>A	NCBI36
NG_008982.1:g.29018C>A
NG_008982.2:g.29023C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-459C>A	ENSP00000388838.2:n.1292-459C>A
ENST00000435065.7:c.1573C>A	ENSP00000402760.2:p.Leu525Met
ENST00000448810.6:c.*353C>A	ENSP00000401860.2:n.*353C>A
ENST00000685543.1:n.1642C>A
ENST00000686757.1:c.*665C>A	ENSP00000510721.1:n.*665C>A
ENST00000686868.1:n.493C>A
ENST00000687740.1:n.4186C>A
ENST00000688151.1:n.2811C>A
ENST00000689271.1:c.1348C>A	ENSP00000510797.1:p.Leu450Met
ENST00000690900.1:c.*665C>A	ENSP00000510703.1:n.*665C>A
ENST00000692212.1:n.4641C>A
ENST00000692355.1:c.754C>A
ENST00000692413.1:c.1483C>A	ENSP00000509374.1:p.Leu495Met
ENST00000692825.1:c.1569C>A	ENSP00000509447.1:n.1569C>A
ENST00000693308.1:c.1549C>A	ENSP00000509770.1:p.Leu517Met
ENST00000693763.1:n.2661C>A
ENST00000245407.8:c.1501C>A MANE Select	ENSP00000245407.3:p.Leu501Met
ENST00000245407.7:c.1501C>A	ENSP00000245407.3:p.Leu501Met
ENST00000435065.6:c.1573C>A	ENSP00000402760.2:p.Leu525Met
ENST00000447841.5:c.345C>A
ENST00000448810.5:c.763C>A
ENST00000461013.5:n.8923C>A
ENST00000475308.1:n.2179C>A
NM_001308122.1:c.1573C>A	NP_001295051.1:p.Leu525Met
NM_003060.3:c.1501C>A	NP_003051.1:p.Leu501Met
XM_011543590.1:c.883C>A	XP_011541892.1:p.Leu295Met
XR_948290.1:n.1627C>A
XM_011543590.2:c.883C>A	XP_011541892.1:p.Leu295Met
XM_017009778.2:c.973C>A	XP_016865267.1:p.Leu325Met
XR_001742215.1:n.1756C>A
XR_001742216.1:n.1775C>A
XR_427718.2:n.1861C>A
XR_948290.2:n.1627C>A
XR_948291.2:n.1855C>A
NM_003060.4:c.1501C>A MANE Select	NP_003051.1:p.Leu501Met
NM_001308122.2:c.1573C>A	NP_001295051.1:p.Leu525Met