Canonical Allele Identifier: CA1583151813

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392492T= , CM000667.2:g.132392492T=	GRCh38
NC_000005.9:g.131728184T= , CM000667.1:g.131728184T=	GRCh37
NC_000005.8:g.131756083T=	NCBI36
NG_008982.1:g.27784T=
NG_008982.2:g.27789T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1168T=	ENSP00000388838.2:p.Phe390=
ENST00000435065.7:c.1399T=	ENSP00000402760.2:p.Phe467=
ENST00000448810.6:c.*179T=	ENSP00000401860.2:n.*179T=
ENST00000685543.1:n.1468T=
ENST00000686757.1:c.*491T=	ENSP00000510721.1:n.*491T=
ENST00000687740.1:n.4012T=
ENST00000688151.1:n.2637T=
ENST00000689271.1:c.1174T=	ENSP00000510797.1:p.Phe392=
ENST00000690900.1:c.*491T=	ENSP00000510703.1:n.*491T=
ENST00000692212.1:n.4467T=
ENST00000692355.1:c.580T=
ENST00000692413.1:c.1309T=	ENSP00000509374.1:p.Phe437=
ENST00000692825.1:c.1395T=	ENSP00000509447.1:n.1395T=
ENST00000693308.1:c.1375T=	ENSP00000509770.1:p.Phe459=
ENST00000693763.1:n.2487T=
ENST00000245407.8:c.1327T= MANE Select	ENSP00000245407.3:p.Phe443=
ENST00000245407.7:c.1327T=	ENSP00000245407.3:p.Phe443=
ENST00000435065.6:c.1399T=	ENSP00000402760.2:p.Phe467=
ENST00000447841.5:c.171T=
ENST00000448810.5:c.589T=
ENST00000461013.5:n.8749T=
ENST00000475308.1:n.2005T=
ENST00000479605.5:n.430T=
NM_001308122.1:c.1399T=	NP_001295051.1:p.Phe467=
NM_003060.3:c.1327T=	NP_003051.1:p.Phe443=
XM_011543590.1:c.709T=	XP_011541892.1:p.Phe237=
XR_948290.1:n.1453T=
XM_011543590.2:c.709T=	XP_011541892.1:p.Phe237=
XM_017009778.2:c.799T=	XP_016865267.1:p.Phe267=
XR_001742215.1:n.1582T=
XR_001742216.1:n.1601T=
XR_427718.2:n.1687T=
XR_948290.2:n.1453T=
XR_948291.2:n.1681T=
NM_003060.4:c.1327T= MANE Select	NP_003051.1:p.Phe443=
NM_001308122.2:c.1399T=	NP_001295051.1:p.Phe467=