Canonical Allele Identifier: CA2675199870

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132393965-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393968_132393969dup , CM000667.2:g.132393968_132393969dup	GRCh38
NC_000005.9:g.131729660_131729661dup , CM000667.1:g.131729660_131729661dup	GRCh37
NC_000005.8:g.131757559_131757560dup	NCBI36
NG_008982.1:g.29260_29261dup
NG_008982.2:g.29265_29266dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-217_1292-216dup	ENSP00000388838.2:n.1292-217_1292-216dup
ENST00000435065.7:c.1658+157_1658+158dup	ENSP00000402760.2:n.1658+157_1658+158dup
ENST00000448810.6:c.*438+157_*438+158dup	ENSP00000401860.2:n.*438+157_*438+158dup
ENST00000685543.1:n.1727+157_1727+158dup
ENST00000686757.1:c.*750+157_*750+158dup	ENSP00000510721.1:n.*750+157_*750+158dup
ENST00000686868.1:n.578+157_578+158dup
ENST00000687740.1:n.4271+157_4271+158dup
ENST00000688151.1:n.2896+157_2896+158dup
ENST00000689271.1:c.1433+157_1433+158dup	ENSP00000510797.1:n.1433+157_1433+158dup
ENST00000690900.1:c.*750+157_*750+158dup	ENSP00000510703.1:n.*750+157_*750+158dup
ENST00000692212.1:n.4726+157_4726+158dup
ENST00000692355.1:c.839+157_839+158dup
ENST00000692413.1:c.1568+157_1568+158dup	ENSP00000509374.1:n.1568+157_1568+158dup
ENST00000692825.1:c.1654+157_1654+158dup	ENSP00000509447.1:n.1654+157_1654+158dup
ENST00000693308.1:c.1634+157_1634+158dup	ENSP00000509770.1:n.1634+157_1634+158dup
ENST00000693763.1:n.2746+157_2746+158dup
ENST00000245407.8:c.1586+157_1586+158dup MANE Select	ENSP00000245407.3:n.1586+157_1586+158dup
ENST00000245407.7:c.1586+157_1586+158dup	ENSP00000245407.3:n.1586+157_1586+158dup
ENST00000435065.6:c.1658+157_1658+158dup	ENSP00000402760.2:n.1658+157_1658+158dup
ENST00000447841.5:c.430+157_430+158dup
ENST00000461013.5:n.9008+157_9008+158dup
ENST00000475308.1:n.2264+157_2264+158dup
NM_001308122.1:c.1658+157_1658+158dup	NP_001295051.1:n.1658+157_1658+158dup
NM_003060.3:c.1586+157_1586+158dup	NP_003051.1:n.1586+157_1586+158dup
XM_011543590.1:c.968+157_968+158dup	XP_011541892.1:n.968+157_968+158dup
XR_948290.1:n.1712+157_1712+158dup
XM_011543590.2:c.968+157_968+158dup	XP_011541892.1:n.968+157_968+158dup
XM_017009778.2:c.1058+157_1058+158dup	XP_016865267.1:n.1058+157_1058+158dup
XR_001742215.1:n.1841+157_1841+158dup
XR_001742216.1:n.1860+157_1860+158dup
XR_427718.2:n.1946+157_1946+158dup
XR_948290.2:n.1712+157_1712+158dup
XR_948291.2:n.1940+157_1940+158dup
NM_003060.4:c.1586+157_1586+158dup MANE Select	NP_003051.1:n.1586+157_1586+158dup
NM_001308122.2:c.1658+157_1658+158dup	NP_001295051.1:n.1658+157_1658+158dup