Canonical Allele Identifier: CA1583144660

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393902C= , CM000667.2:g.132393902C=	GRCh38
NC_000005.9:g.131729594C= , CM000667.1:g.131729594C=	GRCh37
NC_000005.8:g.131757493C=	NCBI36
NG_008982.1:g.29194C=
NG_008982.2:g.29199C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-283C=	ENSP00000388838.2:n.1292-283C=
ENST00000435065.7:c.1658+91C=	ENSP00000402760.2:n.1658+91C=
ENST00000448810.6:c.*438+91C=	ENSP00000401860.2:n.*438+91C=
ENST00000685543.1:n.1727+91C=
ENST00000686757.1:c.*750+91C=	ENSP00000510721.1:n.*750+91C=
ENST00000686868.1:n.578+91C=
ENST00000687740.1:n.4271+91C=
ENST00000688151.1:n.2896+91C=
ENST00000689271.1:c.1433+91C=	ENSP00000510797.1:n.1433+91C=
ENST00000690900.1:c.*750+91C=	ENSP00000510703.1:n.*750+91C=
ENST00000692212.1:n.4726+91C=
ENST00000692355.1:c.839+91C=
ENST00000692413.1:c.1568+91C=	ENSP00000509374.1:n.1568+91C=
ENST00000692825.1:c.1654+91C=	ENSP00000509447.1:n.1654+91C=
ENST00000693308.1:c.1634+91C=	ENSP00000509770.1:n.1634+91C=
ENST00000693763.1:n.2746+91C=
ENST00000245407.8:c.1586+91C= MANE Select	ENSP00000245407.3:n.1586+91C=
ENST00000245407.7:c.1586+91C=	ENSP00000245407.3:n.1586+91C=
ENST00000435065.6:c.1658+91C=	ENSP00000402760.2:n.1658+91C=
ENST00000447841.5:c.430+91C=
ENST00000461013.5:n.9008+91C=
ENST00000475308.1:n.2264+91C=
NM_001308122.1:c.1658+91C=	NP_001295051.1:n.1658+91C=
NM_003060.3:c.1586+91C=	NP_003051.1:n.1586+91C=
XM_011543590.1:c.968+91C=	XP_011541892.1:n.968+91C=
XR_948290.1:n.1712+91C=
XM_011543590.2:c.968+91C=	XP_011541892.1:n.968+91C=
XM_017009778.2:c.1058+91C=	XP_016865267.1:n.1058+91C=
XR_001742215.1:n.1841+91C=
XR_001742216.1:n.1860+91C=
XR_427718.2:n.1946+91C=
XR_948290.2:n.1712+91C=
XR_948291.2:n.1940+91C=
NM_003060.4:c.1586+91C= MANE Select	NP_003051.1:n.1586+91C=
NM_001308122.2:c.1658+91C=	NP_001295051.1:n.1658+91C=