Canonical Allele Identifier: CA127208734

Gene: SLC22A5

Linked Data

• ClinVar Variation Id: 957604
• ClinVar RCV Id: RCV001230608
• dbSNP Id: rs558978831
• gnomAD v3: 5-132384163-G-A
• gnomAD v4: 5-132384163-G-A
• MyVariant Identifiers: chr5:g.131719855G>A (hg19) ; chr5:g.132384163G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384163G>A , CM000667.2:g.132384163G>A	GRCh38
NC_000005.9:g.131719855G>A , CM000667.1:g.131719855G>A	GRCh37
NC_000005.8:g.131747754G>A	NCBI36
NG_008982.1:g.19455G>A
NG_008982.2:g.19460G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.514G>A	ENSP00000388838.2:p.Val172Met
ENST00000435065.7:c.586G>A	ENSP00000402760.2:p.Val196Met
ENST00000448810.6:c.514G>A	ENSP00000401860.2:p.Val172Met
ENST00000686757.1:c.514G>A	ENSP00000510721.1:p.Val172Met
ENST00000687740.1:n.648G>A
ENST00000688151.1:n.1693G>A
ENST00000689271.1:c.514G>A	ENSP00000510797.1:p.Val172Met
ENST00000690900.1:c.514G>A	ENSP00000510703.1:p.Val172Met
ENST00000692355.1:c.66G>A
ENST00000692413.1:c.514G>A	ENSP00000509374.1:p.Val172Met
ENST00000692825.1:c.582G>A	ENSP00000509447.1:n.582G>A
ENST00000693308.1:c.514G>A	ENSP00000509770.1:p.Val172Met
ENST00000693763.1:n.648G>A
ENST00000245407.8:c.514G>A MANE Select	ENSP00000245407.3:p.Val172Met
ENST00000245407.7:c.514G>A	ENSP00000245407.3:p.Val172Met
ENST00000415928.5:c.283G>A	ENSP00000388838.1:p.Val95Met
ENST00000435065.6:c.586G>A	ENSP00000402760.2:p.Val196Met
ENST00000437841.6:c.394-1165G>A	ENSP00000400553.1:n.394-1165G>A
ENST00000461013.5:n.7936G>A
NM_001308122.1:c.586G>A	NP_001295051.1:p.Val196Met
NM_003060.3:c.514G>A	NP_003051.1:p.Val172Met
XR_427718.1:n.855G>A
XR_948290.1:n.855G>A
XR_948291.1:n.855G>A
XM_011543590.2:c.-118G>A	XP_011541892.1:n.-118G>A
XM_017009778.2:c.-15G>A	XP_016865267.1:n.-15G>A
XR_001742215.1:n.855G>A
XR_001742216.1:n.855G>A
XR_427718.2:n.855G>A
XR_948290.2:n.855G>A
XR_948291.2:n.855G>A
NM_003060.4:c.514G>A MANE Select	NP_003051.1:p.Val172Met
NM_001308122.2:c.586G>A	NP_001295051.1:p.Val196Met