Canonical Allele Identifier: CA3403933

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384280T>C , CM000667.2:g.132384280T>C	GRCh38
NC_000005.9:g.131719972T>C , CM000667.1:g.131719972T>C	GRCh37
NC_000005.8:g.131747871T>C	NCBI36
NG_008982.1:g.19572T>C
NG_008982.2:g.19577T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003060.4:c.631T>C MANE Select	NP_003051.1:p.Tyr211His
ENST00000245407.8:c.631T>C MANE Select	ENSP00000245407.3:p.Tyr211His
NM_001308122.1:c.703T>C	NP_001295051.1:p.Tyr235His
NM_001308122.2:c.703T>C	NP_001295051.1:p.Tyr235His
NM_003060.3:c.631T>C	NP_003051.1:p.Tyr211His
ENST00000245407.7:c.631T>C	ENSP00000245407.3:p.Tyr211His
ENST00000415928.5:c.400T>C	ENSP00000388838.1:p.Tyr134His
ENST00000415928.6:c.631T>C	ENSP00000388838.2:p.Tyr211His
ENST00000435065.6:c.703T>C	ENSP00000402760.2:p.Tyr235His
ENST00000435065.7:c.703T>C	ENSP00000402760.2:p.Tyr235His
ENST00000437841.6:c.394-1048T>C	ENSP00000400553.1:n.394-1048T>C
ENST00000448810.6:c.631T>C	ENSP00000401860.2:p.Tyr211His
ENST00000461013.5:n.8053T>C
ENST00000686757.1:c.631T>C	ENSP00000510721.1:p.Tyr211His
ENST00000687740.1:n.765T>C
ENST00000688151.1:n.1810T>C
ENST00000689271.1:c.631T>C	ENSP00000510797.1:p.Tyr211His
ENST00000690900.1:c.631T>C	ENSP00000510703.1:p.Tyr211His
ENST00000692355.1:c.183T>C
ENST00000692413.1:c.631T>C	ENSP00000509374.1:p.Tyr211His
ENST00000692825.1:c.699T>C	ENSP00000509447.1:n.699T>C
ENST00000693308.1:c.631T>C	ENSP00000509770.1:p.Tyr211His
ENST00000693763.1:n.765T>C
XM_011543590.1:c.-1T>C	XP_011541892.1:n.-1T>C
XM_011543590.2:c.-1T>C	XP_011541892.1:n.-1T>C
XM_017009778.2:c.103T>C	XP_016865267.1:p.Tyr35His
XR_001742215.1:n.972T>C
XR_001742216.1:n.972T>C
XR_427718.1:n.972T>C
XR_427718.2:n.972T>C
XR_948290.1:n.972T>C
XR_948290.2:n.972T>C
XR_948291.1:n.972T>C
XR_948291.2:n.972T>C