Canonical Allele Identifier: CA360807655

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726491G>T (hg19) ; chr5:g.132390799G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390799G>T , CM000667.2:g.132390799G>T	GRCh38
NC_000005.9:g.131726491G>T , CM000667.1:g.131726491G>T	GRCh37
NC_000005.8:g.131754390G>T	NCBI36
NG_008982.1:g.26091G>T
NG_008982.2:g.26096G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1003G>T	ENSP00000388838.2:p.Val335Leu
ENST00000435065.7:c.1234G>T	ENSP00000402760.2:p.Val412Leu
ENST00000448810.6:c.*14G>T	ENSP00000401860.2:n.*14G>T
ENST00000685543.1:n.1303G>T
ENST00000686757.1:c.*326G>T	ENSP00000510721.1:n.*326G>T
ENST00000687740.1:n.3847G>T
ENST00000688151.1:n.2472G>T
ENST00000689271.1:c.1009G>T	ENSP00000510797.1:p.Val337Leu
ENST00000690900.1:c.*326G>T	ENSP00000510703.1:n.*326G>T
ENST00000692212.1:n.2774G>T
ENST00000692355.1:c.415G>T
ENST00000692413.1:c.1144G>T	ENSP00000509374.1:p.Val382Leu
ENST00000692825.1:c.1230G>T	ENSP00000509447.1:n.1230G>T
ENST00000693308.1:c.1210G>T	ENSP00000509770.1:p.Val404Leu
ENST00000693763.1:n.2322G>T
ENST00000245407.8:c.1162G>T MANE Select	ENSP00000245407.3:p.Val388Leu
ENST00000245407.7:c.1162G>T	ENSP00000245407.3:p.Val388Leu
ENST00000435065.6:c.1234G>T	ENSP00000402760.2:p.Val412Leu
ENST00000447841.5:c.112-1634G>T
ENST00000448810.5:c.424G>T
ENST00000461013.5:n.8584G>T
ENST00000475308.1:n.1840G>T
ENST00000479605.5:n.265G>T
NM_001308122.1:c.1234G>T	NP_001295051.1:p.Val412Leu
NM_003060.3:c.1162G>T	NP_003051.1:p.Val388Leu
XM_011543590.1:c.544G>T	XP_011541892.1:p.Val182Leu
XR_427718.1:n.1522G>T
XR_948290.1:n.1394-1634G>T
XR_948291.1:n.1516G>T
XM_011543590.2:c.544G>T	XP_011541892.1:p.Val182Leu
XM_017009778.2:c.634G>T	XP_016865267.1:p.Val212Leu
XR_001742215.1:n.1417G>T
XR_001742216.1:n.1436G>T
XR_427718.2:n.1522G>T
XR_948290.2:n.1394-1634G>T
XR_948291.2:n.1516G>T
NM_003060.4:c.1162G>T MANE Select	NP_003051.1:p.Val388Leu
NM_001308122.2:c.1234G>T	NP_001295051.1:p.Val412Leu