Canonical Allele Identifier: CA360807417

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726396T>G (hg19) ; chr5:g.132390704T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390704T>G , CM000667.2:g.132390704T>G	GRCh38
NC_000005.9:g.131726396T>G , CM000667.1:g.131726396T>G	GRCh37
NC_000005.8:g.131754295T>G	NCBI36
NG_008982.1:g.25996T>G
NG_008982.2:g.26001T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.908T>G	ENSP00000388838.2:p.Val303Gly
ENST00000435065.7:c.1139T>G	ENSP00000402760.2:p.Val380Gly
ENST00000448810.6:c.1053-72T>G	ENSP00000401860.2:n.1053-72T>G
ENST00000685543.1:n.1208T>G
ENST00000686757.1:c.*231T>G	ENSP00000510721.1:n.*231T>G
ENST00000687740.1:n.3752T>G
ENST00000688151.1:n.2377T>G
ENST00000689271.1:c.914T>G	ENSP00000510797.1:p.Val305Gly
ENST00000690900.1:c.*231T>G	ENSP00000510703.1:n.*231T>G
ENST00000692212.1:n.2679T>G
ENST00000692355.1:c.320T>G
ENST00000692413.1:c.1049T>G	ENSP00000509374.1:p.Val350Gly
ENST00000692825.1:c.1135T>G	ENSP00000509447.1:n.1135T>G
ENST00000693308.1:c.1115T>G	ENSP00000509770.1:p.Val372Gly
ENST00000693763.1:n.2227T>G
ENST00000245407.8:c.1067T>G MANE Select	ENSP00000245407.3:p.Val356Gly
ENST00000245407.7:c.1067T>G	ENSP00000245407.3:p.Val356Gly
ENST00000435065.6:c.1139T>G	ENSP00000402760.2:p.Val380Gly
ENST00000447841.5:c.111+1683T>G
ENST00000448810.5:c.401-72T>G
ENST00000461013.5:n.8489T>G
ENST00000475308.1:n.1745T>G
ENST00000479605.5:n.170T>G
NM_001308122.1:c.1139T>G	NP_001295051.1:p.Val380Gly
NM_003060.3:c.1067T>G	NP_003051.1:p.Val356Gly
XM_011543590.1:c.449T>G	XP_011541892.1:p.Val150Gly
XR_427718.1:n.1427T>G
XR_948290.1:n.1393+1683T>G
XR_948291.1:n.1421T>G
XM_011543590.2:c.449T>G	XP_011541892.1:p.Val150Gly
XM_017009778.2:c.539T>G	XP_016865267.1:p.Val180Gly
XR_001742215.1:n.1394-72T>G
XR_001742216.1:n.1413-72T>G
XR_427718.2:n.1427T>G
XR_948290.2:n.1393+1683T>G
XR_948291.2:n.1421T>G
NM_003060.4:c.1067T>G MANE Select	NP_003051.1:p.Val356Gly
NM_001308122.2:c.1139T>G	NP_001295051.1:p.Val380Gly