Canonical Allele Identifier: CA446339965

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726565T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390873T>C , CM000667.2:g.132390873T>C	GRCh38
NC_000005.9:g.131726565T>C , CM000667.1:g.131726565T>C	GRCh37
NC_000005.8:g.131754464T>C	NCBI36
NG_008982.1:g.26165T>C
NG_008982.2:g.26170T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1077T>C	ENSP00000388838.2:p.Ser359=
ENST00000435065.7:c.1308T>C	ENSP00000402760.2:p.Ser436=
ENST00000448810.6:c.*88T>C	ENSP00000401860.2:n.*88T>C
ENST00000685543.1:n.1377T>C
ENST00000686757.1:c.*400T>C	ENSP00000510721.1:n.*400T>C
ENST00000687740.1:n.3921T>C
ENST00000688151.1:n.2546T>C
ENST00000689271.1:c.1083T>C	ENSP00000510797.1:p.Ser361=
ENST00000690900.1:c.*400T>C	ENSP00000510703.1:n.*400T>C
ENST00000692212.1:n.2848T>C
ENST00000692355.1:c.489T>C
ENST00000692413.1:c.1218T>C	ENSP00000509374.1:p.Ser406=
ENST00000692825.1:c.1304T>C	ENSP00000509447.1:n.1304T>C
ENST00000693308.1:c.1284T>C	ENSP00000509770.1:p.Ser428=
ENST00000693763.1:n.2396T>C
ENST00000245407.8:c.1236T>C MANE Select	ENSP00000245407.3:p.Ser412=
ENST00000245407.7:c.1236T>C	ENSP00000245407.3:p.Ser412=
ENST00000435065.6:c.1308T>C	ENSP00000402760.2:p.Ser436=
ENST00000447841.5:c.112-1560T>C
ENST00000448810.5:c.498T>C
ENST00000461013.5:n.8658T>C
ENST00000475308.1:n.1914T>C
ENST00000479605.5:n.339T>C
NM_001308122.1:c.1308T>C	NP_001295051.1:p.Ser436=
NM_003060.3:c.1236T>C	NP_003051.1:p.Ser412=
XM_011543590.1:c.618T>C	XP_011541892.1:p.Ser206=
XR_427718.1:n.1596T>C
XR_948290.1:n.1394-1560T>C
XR_948291.1:n.1590T>C
XM_011543590.2:c.618T>C	XP_011541892.1:p.Ser206=
XM_017009778.2:c.708T>C	XP_016865267.1:p.Ser236=
XR_001742215.1:n.1491T>C
XR_001742216.1:n.1510T>C
XR_427718.2:n.1596T>C
XR_948290.2:n.1394-1560T>C
XR_948291.2:n.1590T>C
NM_003060.4:c.1236T>C MANE Select	NP_003051.1:p.Ser412=
NM_001308122.2:c.1308T>C	NP_001295051.1:p.Ser436=