Canonical Allele Identifier: CA1583150058

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390794_132390795delinsCA , CM000667.2:g.132390794_132390795delinsCA	GRCh38
NC_000005.9:g.131726486_131726487delinsCA , CM000667.1:g.131726486_131726487delinsCA	GRCh37
NC_000005.8:g.131754385_131754386delinsCA	NCBI36
NG_008982.1:g.26086_26087delinsCA
NG_008982.2:g.26091_26092delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.998_999delinsCA	ENSP00000388838.2:p.Ala333=
ENST00000435065.7:c.1229_1230delinsCA	ENSP00000402760.2:p.Ala410=
ENST00000448810.6:c.*9_*10delinsCA	ENSP00000401860.2:n.*9_*10delinsCA
ENST00000685543.1:n.1298_1299delinsCA
ENST00000686757.1:c.*321_*322delinsCA	ENSP00000510721.1:n.*321_*322delinsCA
ENST00000687740.1:n.3842_3843delinsCA
ENST00000688151.1:n.2467_2468delinsCA
ENST00000689271.1:c.1004_1005delinsCA	ENSP00000510797.1:p.Ala335=
ENST00000690900.1:c.*321_*322delinsCA	ENSP00000510703.1:n.*321_*322delinsCA
ENST00000692212.1:n.2769_2770delinsCA
ENST00000692355.1:c.410_411delinsCA
ENST00000692413.1:c.1139_1140delinsCA	ENSP00000509374.1:p.Ala380=
ENST00000692825.1:c.1225_1226delinsCA	ENSP00000509447.1:n.1225_1226delinsCA
ENST00000693308.1:c.1205_1206delinsCA	ENSP00000509770.1:p.Ala402=
ENST00000693763.1:n.2317_2318delinsCA
ENST00000245407.8:c.1157_1158delinsCA MANE Select	ENSP00000245407.3:p.Ala386=
ENST00000245407.7:c.1157_1158delinsCA	ENSP00000245407.3:p.Ala386=
ENST00000435065.6:c.1229_1230delinsCA	ENSP00000402760.2:p.Ala410=
ENST00000447841.5:c.112-1639_112-1638delinsCA
ENST00000448810.5:c.419_420delinsCA
ENST00000461013.5:n.8579_8580delinsCA
ENST00000475308.1:n.1835_1836delinsCA
ENST00000479605.5:n.260_261delinsCA
NM_001308122.1:c.1229_1230delinsCA	NP_001295051.1:p.Ala410=
NM_003060.3:c.1157_1158delinsCA	NP_003051.1:p.Ala386=
XM_011543590.1:c.539_540delinsCA	XP_011541892.1:p.Ala180=
XR_427718.1:n.1517_1518delinsCA
XR_948290.1:n.1394-1639_1394-1638delinsCA
XR_948291.1:n.1511_1512delinsCA
XM_011543590.2:c.539_540delinsCA	XP_011541892.1:p.Ala180=
XM_017009778.2:c.629_630delinsCA	XP_016865267.1:p.Ala210=
XR_001742215.1:n.1412_1413delinsCA
XR_001742216.1:n.1431_1432delinsCA
XR_427718.2:n.1517_1518delinsCA
XR_948290.2:n.1394-1639_1394-1638delinsCA
XR_948291.2:n.1511_1512delinsCA
NM_003060.4:c.1157_1158delinsCA MANE Select	NP_003051.1:p.Ala386=
NM_001308122.2:c.1229_1230delinsCA	NP_001295051.1:p.Ala410=