Canonical Allele Identifier: CA360807841

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726582A>T (hg19) ; chr5:g.132390890A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390890A>T , CM000667.2:g.132390890A>T	GRCh38
NC_000005.9:g.131726582A>T , CM000667.1:g.131726582A>T	GRCh37
NC_000005.8:g.131754481A>T	NCBI36
NG_008982.1:g.26182A>T
NG_008982.2:g.26187A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1094A>T	ENSP00000388838.2:p.Gln365Leu
ENST00000435065.7:c.1325A>T	ENSP00000402760.2:p.Gln442Leu
ENST00000448810.6:c.*105A>T	ENSP00000401860.2:n.*105A>T
ENST00000685543.1:n.1394A>T
ENST00000686757.1:c.*417A>T	ENSP00000510721.1:n.*417A>T
ENST00000687740.1:n.3938A>T
ENST00000688151.1:n.2563A>T
ENST00000689271.1:c.1100A>T	ENSP00000510797.1:p.Gln367Leu
ENST00000690900.1:c.*417A>T	ENSP00000510703.1:n.*417A>T
ENST00000692212.1:n.2865A>T
ENST00000692355.1:c.506A>T
ENST00000692413.1:c.1235A>T	ENSP00000509374.1:p.Gln412Leu
ENST00000692825.1:c.1321A>T	ENSP00000509447.1:n.1321A>T
ENST00000693308.1:c.1301A>T	ENSP00000509770.1:p.Gln434Leu
ENST00000693763.1:n.2413A>T
ENST00000245407.8:c.1253A>T MANE Select	ENSP00000245407.3:p.Gln418Leu
ENST00000245407.7:c.1253A>T	ENSP00000245407.3:p.Gln418Leu
ENST00000435065.6:c.1325A>T	ENSP00000402760.2:p.Gln442Leu
ENST00000447841.5:c.112-1543A>T
ENST00000448810.5:c.515A>T
ENST00000461013.5:n.8675A>T
ENST00000475308.1:n.1931A>T
ENST00000479605.5:n.356A>T
NM_001308122.1:c.1325A>T	NP_001295051.1:p.Gln442Leu
NM_003060.3:c.1253A>T	NP_003051.1:p.Gln418Leu
XM_011543590.1:c.635A>T	XP_011541892.1:p.Gln212Leu
XR_427718.1:n.1613A>T
XR_948290.1:n.1394-1543A>T
XR_948291.1:n.1607A>T
XM_011543590.2:c.635A>T	XP_011541892.1:p.Gln212Leu
XM_017009778.2:c.725A>T	XP_016865267.1:p.Gln242Leu
XR_001742215.1:n.1508A>T
XR_001742216.1:n.1527A>T
XR_427718.2:n.1613A>T
XR_948290.2:n.1394-1543A>T
XR_948291.2:n.1607A>T
NM_003060.4:c.1253A>T MANE Select	NP_003051.1:p.Gln418Leu
NM_001308122.2:c.1325A>T	NP_001295051.1:p.Gln442Leu