Canonical Allele Identifier: CA2841621153

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369944G>T , CM000667.2:g.132369944G>T	GRCh38
NC_000005.9:g.131705636G>T , CM000667.1:g.131705636G>T	GRCh37
NC_000005.8:g.131733535G>T	NCBI36
NG_008982.1:g.5236G>T
NG_008982.2:g.5241G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.-29G>T	ENSP00000388838.2:n.-29G>T
ENST00000435065.7:c.-29G>T	ENSP00000402760.2:n.-29G>T
ENST00000448810.6:c.-29G>T	ENSP00000401860.2:n.-29G>T
ENST00000686757.1:c.-29G>T	ENSP00000510721.1:n.-29G>T
ENST00000687740.1:n.106G>T
ENST00000689271.1:c.-29G>T	ENSP00000510797.1:n.-29G>T
ENST00000690900.1:c.-29G>T	ENSP00000510703.1:n.-29G>T
ENST00000692413.1:c.-29G>T	ENSP00000509374.1:n.-29G>T
ENST00000693308.1:c.-29G>T	ENSP00000509770.1:n.-29G>T
ENST00000693763.1:n.106G>T
ENST00000245407.8:c.-29G>T MANE Select	ENSP00000245407.3:n.-29G>T
ENST00000245407.7:c.-29G>T	ENSP00000245407.3:n.-29G>T
ENST00000437841.6:c.-29G>T	ENSP00000400553.1:n.-29G>T
NM_001308122.1:c.-29G>T	NP_001295051.1:n.-29G>T
NM_003060.3:c.-29G>T	NP_003051.1:n.-29G>T
XR_427718.1:n.241G>T
XR_948290.1:n.241G>T
XR_948291.1:n.241G>T
XR_001742215.1:n.241G>T
XR_001742216.1:n.241G>T
XR_427718.2:n.241G>T
XR_948290.2:n.241G>T
XR_948291.2:n.241G>T
NM_003060.4:c.-29G>T MANE Select	NP_003051.1:n.-29G>T
NM_001308122.2:c.-29G>T	NP_001295051.1:n.-29G>T