Canonical Allele Identifier: CA1583144524

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393741A= , CM000667.2:g.132393741A=	GRCh38
NC_000005.9:g.131729433A= , CM000667.1:g.131729433A=	GRCh37
NC_000005.8:g.131757332A=	NCBI36
NG_008982.1:g.29033A=
NG_008982.2:g.29038A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-444A=	ENSP00000388838.2:n.1292-444A=
ENST00000435065.7:c.1588A=	ENSP00000402760.2:p.Thr530=
ENST00000448810.6:c.*368A=	ENSP00000401860.2:n.*368A=
ENST00000685543.1:n.1657A=
ENST00000686757.1:c.*680A=	ENSP00000510721.1:n.*680A=
ENST00000686868.1:n.508A=
ENST00000687740.1:n.4201A=
ENST00000688151.1:n.2826A=
ENST00000689271.1:c.1363A=	ENSP00000510797.1:p.Thr455=
ENST00000690900.1:c.*680A=	ENSP00000510703.1:n.*680A=
ENST00000692212.1:n.4656A=
ENST00000692355.1:c.769A=
ENST00000692413.1:c.1498A=	ENSP00000509374.1:p.Thr500=
ENST00000692825.1:c.1584A=	ENSP00000509447.1:n.1584A=
ENST00000693308.1:c.1564A=	ENSP00000509770.1:p.Thr522=
ENST00000693763.1:n.2676A=
ENST00000245407.8:c.1516A= MANE Select	ENSP00000245407.3:p.Thr506=
ENST00000245407.7:c.1516A=	ENSP00000245407.3:p.Thr506=
ENST00000435065.6:c.1588A=	ENSP00000402760.2:p.Thr530=
ENST00000447841.5:c.360A=
ENST00000448810.5:c.778A=
ENST00000461013.5:n.8938A=
ENST00000475308.1:n.2194A=
NM_001308122.1:c.1588A=	NP_001295051.1:p.Thr530=
NM_003060.3:c.1516A=	NP_003051.1:p.Thr506=
XM_011543590.1:c.898A=	XP_011541892.1:p.Thr300=
XR_948290.1:n.1642A=
XM_011543590.2:c.898A=	XP_011541892.1:p.Thr300=
XM_017009778.2:c.988A=	XP_016865267.1:p.Thr330=
XR_001742215.1:n.1771A=
XR_001742216.1:n.1790A=
XR_427718.2:n.1876A=
XR_948290.2:n.1642A=
XR_948291.2:n.1870A=
NM_003060.4:c.1516A= MANE Select	NP_003051.1:p.Thr506=
NM_001308122.2:c.1588A=	NP_001295051.1:p.Thr530=