Canonical Allele Identifier: CA1583144301

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393593G= , CM000667.2:g.132393593G=	GRCh38
NC_000005.9:g.131729285G= , CM000667.1:g.131729285G=	GRCh37
NC_000005.8:g.131757184G=	NCBI36
NG_008982.1:g.28885G=
NG_008982.2:g.28890G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-592G=	ENSP00000388838.2:n.1292-592G=
ENST00000435065.7:c.1523-83G=	ENSP00000402760.2:n.1523-83G=
ENST00000448810.6:c.*303-83G=	ENSP00000401860.2:n.*303-83G=
ENST00000685543.1:n.1592-83G=
ENST00000686757.1:c.*615-83G=	ENSP00000510721.1:n.*615-83G=
ENST00000686868.1:n.360G=
ENST00000687740.1:n.4136-83G=
ENST00000688151.1:n.2761-83G=
ENST00000689271.1:c.1298-83G=	ENSP00000510797.1:n.1298-83G=
ENST00000690900.1:c.*615-83G=	ENSP00000510703.1:n.*615-83G=
ENST00000692212.1:n.4591-83G=
ENST00000692355.1:c.704-83G=
ENST00000692413.1:c.1433-83G=	ENSP00000509374.1:n.1433-83G=
ENST00000692825.1:c.1519-83G=	ENSP00000509447.1:n.1519-83G=
ENST00000693308.1:c.1499-83G=	ENSP00000509770.1:n.1499-83G=
ENST00000693763.1:n.2611-83G=
ENST00000245407.8:c.1451-83G= MANE Select	ENSP00000245407.3:n.1451-83G=
ENST00000245407.7:c.1451-83G=	ENSP00000245407.3:n.1451-83G=
ENST00000435065.6:c.1523-83G=	ENSP00000402760.2:n.1523-83G=
ENST00000447841.5:c.295-83G=
ENST00000448810.5:c.713-83G=
ENST00000461013.5:n.8873-83G=
ENST00000475308.1:n.2129-83G=
ENST00000479605.5:n.554-83G=
NM_001308122.1:c.1523-83G=	NP_001295051.1:n.1523-83G=
NM_003060.3:c.1451-83G=	NP_003051.1:n.1451-83G=
XM_011543590.1:c.833-83G=	XP_011541892.1:n.833-83G=
XR_948290.1:n.1577-83G=
XM_011543590.2:c.833-83G=	XP_011541892.1:n.833-83G=
XM_017009778.2:c.923-83G=	XP_016865267.1:n.923-83G=
XR_001742215.1:n.1706-83G=
XR_001742216.1:n.1725-83G=
XR_427718.2:n.1811-83G=
XR_948290.2:n.1577-83G=
XR_948291.2:n.1805-83G=
NM_003060.4:c.1451-83G= MANE Select	NP_003051.1:n.1451-83G=
NM_001308122.2:c.1523-83G=	NP_001295051.1:n.1523-83G=