Canonical Allele Identifier: CA2675203783

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132390555-A-ATGAAGTAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390555_132390556insTGAAGTAAG , CM000667.2:g.132390555_132390556insTGAAGTAAG	GRCh38
NC_000005.9:g.131726247_131726248insTGAAGTAAG , CM000667.1:g.131726247_131726248insTGAAGTAAG	GRCh37
NC_000005.8:g.131754146_131754147insTGAAGTAAG	NCBI36
NG_008982.1:g.25847_25848insTGAAGTAAG
NG_008982.2:g.25852_25853insTGAAGTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-135_894-134insTGAAGTAAG	ENSP00000388838.2:n.894-135_894-134insTGAAGTAAG
ENST00000435065.7:c.1125-135_1125-134insTGAAGTAAG	ENSP00000402760.2:n.1125-135_1125-134insTGAAGTAAG
ENST00000448810.6:c.1053-221_1053-220insTGAAGTAAG	ENSP00000401860.2:n.1053-221_1053-220insTGAAGTAAG
ENST00000685543.1:n.1194-135_1194-134insTGAAGTAAG
ENST00000686757.1:c.*217-135_*217-134insTGAAGTAAG	ENSP00000510721.1:n.*217-135_*217-134insTGAAGTAAG
ENST00000687740.1:n.3738-135_3738-134insTGAAGTAAG
ENST00000688151.1:n.2363-135_2363-134insTGAAGTAAG
ENST00000689271.1:c.900-135_900-134insTGAAGTAAG	ENSP00000510797.1:n.900-135_900-134insTGAAGTAAG
ENST00000690900.1:c.*217-135_*217-134insTGAAGTAAG	ENSP00000510703.1:n.*217-135_*217-134insTGAAGTAAG
ENST00000692212.1:n.2530_2531insTGAAGTAAG
ENST00000692355.1:c.306-135_306-134insTGAAGTAAG
ENST00000692413.1:c.1035-135_1035-134insTGAAGTAAG	ENSP00000509374.1:n.1035-135_1035-134insTGAAGTAAG
ENST00000692825.1:c.1121-135_1121-134insTGAAGTAAG	ENSP00000509447.1:n.1121-135_1121-134insTGAAGTAAG
ENST00000693308.1:c.1101-135_1101-134insTGAAGTAAG	ENSP00000509770.1:n.1101-135_1101-134insTGAAGTAAG
ENST00000693763.1:n.2213-135_2213-134insTGAAGTAAG
ENST00000245407.8:c.1053-135_1053-134insTGAAGTAAG MANE Select	ENSP00000245407.3:n.1053-135_1053-134insTGAAGTAAG
ENST00000245407.7:c.1053-135_1053-134insTGAAGTAAG	ENSP00000245407.3:n.1053-135_1053-134insTGAAGTAAG
ENST00000435065.6:c.1125-135_1125-134insTGAAGTAAG	ENSP00000402760.2:n.1125-135_1125-134insTGAAGTAAG
ENST00000447841.5:c.111+1534_111+1535insTGAAGTAAG
ENST00000448810.5:c.401-221_401-220insTGAAGTAAG
ENST00000461013.5:n.8475-135_8475-134insTGAAGTAAG
ENST00000475308.1:n.1596_1597insTGAAGTAAG
ENST00000479605.5:n.156-135_156-134insTGAAGTAAG
NM_001308122.1:c.1125-135_1125-134insTGAAGTAAG	NP_001295051.1:n.1125-135_1125-134insTGAAGTAAG
NM_003060.3:c.1053-135_1053-134insTGAAGTAAG	NP_003051.1:n.1053-135_1053-134insTGAAGTAAG
XM_011543590.1:c.435-135_435-134insTGAAGTAAG	XP_011541892.1:n.435-135_435-134insTGAAGTAAG
XR_427718.1:n.1413-135_1413-134insTGAAGTAAG
XR_948290.1:n.1393+1534_1393+1535insTGAAGTAAG
XR_948291.1:n.1407-135_1407-134insTGAAGTAAG
XM_011543590.2:c.435-135_435-134insTGAAGTAAG	XP_011541892.1:n.435-135_435-134insTGAAGTAAG
XM_017009778.2:c.525-135_525-134insTGAAGTAAG	XP_016865267.1:n.525-135_525-134insTGAAGTAAG
XR_001742215.1:n.1394-221_1394-220insTGAAGTAAG
XR_001742216.1:n.1413-221_1413-220insTGAAGTAAG
XR_427718.2:n.1413-135_1413-134insTGAAGTAAG
XR_948290.2:n.1393+1534_1393+1535insTGAAGTAAG
XR_948291.2:n.1407-135_1407-134insTGAAGTAAG
NM_003060.4:c.1053-135_1053-134insTGAAGTAAG MANE Select	NP_003051.1:n.1053-135_1053-134insTGAAGTAAG
NM_001308122.2:c.1125-135_1125-134insTGAAGTAAG	NP_001295051.1:n.1125-135_1125-134insTGAAGTAAG