Canonical Allele Identifier: CA360807618

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726474T>A (hg19) ; chr5:g.132390782T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390782T>A , CM000667.2:g.132390782T>A	GRCh38
NC_000005.9:g.131726474T>A , CM000667.1:g.131726474T>A	GRCh37
NC_000005.8:g.131754373T>A	NCBI36
NG_008982.1:g.26074T>A
NG_008982.2:g.26079T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.986T>A	ENSP00000388838.2:p.Val329Asp
ENST00000435065.7:c.1217T>A	ENSP00000402760.2:p.Val406Asp
ENST00000448810.6:c.1059T>A	ENSP00000401860.2:p.Gly353=
ENST00000685543.1:n.1286T>A
ENST00000686757.1:c.*309T>A	ENSP00000510721.1:n.*309T>A
ENST00000687740.1:n.3830T>A
ENST00000688151.1:n.2455T>A
ENST00000689271.1:c.992T>A	ENSP00000510797.1:p.Val331Asp
ENST00000690900.1:c.*309T>A	ENSP00000510703.1:n.*309T>A
ENST00000692212.1:n.2757T>A
ENST00000692355.1:c.398T>A
ENST00000692413.1:c.1127T>A	ENSP00000509374.1:p.Val376Asp
ENST00000692825.1:c.1213T>A	ENSP00000509447.1:n.1213T>A
ENST00000693308.1:c.1193T>A	ENSP00000509770.1:p.Val398Asp
ENST00000693763.1:n.2305T>A
ENST00000245407.8:c.1145T>A MANE Select	ENSP00000245407.3:p.Val382Asp
ENST00000245407.7:c.1145T>A	ENSP00000245407.3:p.Val382Asp
ENST00000435065.6:c.1217T>A	ENSP00000402760.2:p.Val406Asp
ENST00000447841.5:c.112-1651T>A
ENST00000448810.5:c.407T>A
ENST00000461013.5:n.8567T>A
ENST00000475308.1:n.1823T>A
ENST00000479605.5:n.248T>A
NM_001308122.1:c.1217T>A	NP_001295051.1:p.Val406Asp
NM_003060.3:c.1145T>A	NP_003051.1:p.Val382Asp
XM_011543590.1:c.527T>A	XP_011541892.1:p.Val176Asp
XR_427718.1:n.1505T>A
XR_948290.1:n.1394-1651T>A
XR_948291.1:n.1499T>A
XM_011543590.2:c.527T>A	XP_011541892.1:p.Val176Asp
XM_017009778.2:c.617T>A	XP_016865267.1:p.Val206Asp
XR_001742215.1:n.1400T>A
XR_001742216.1:n.1419T>A
XR_427718.2:n.1505T>A
XR_948290.2:n.1394-1651T>A
XR_948291.2:n.1499T>A
NM_003060.4:c.1145T>A MANE Select	NP_003051.1:p.Val382Asp
NM_001308122.2:c.1217T>A	NP_001295051.1:p.Val406Asp