Canonical Allele Identifier: CA1335855840

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233682134T= , CM000664.2:g.233682134T= GRCh38
NC_000002.11:g.234590780T= , CM000664.1:g.234590780T= GRCh37
NC_000002.10:g.234255519T= NCBI36
NG_002601.2:g.97391T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344644.10:c.855+44757T= (UGT1A10) MANE Select ENSP00000343838.5:n.855+44757T=
ENST00000373426.4:c.197T= (UGT1A7) MANE Select ENSP00000362525.3:p.Leu66=
ENST00000373450.5:c.855+63572T= (UGT1A8) MANE Select ENSP00000362549.4:n.855+63572T=
ENST00000354728.5:c.855+9345T= (UGT1A9) MANE Select ENSP00000346768.4:n.855+9345T=
ENST00000344644.9:c.855+44757T= (UGT1A10) ENSP00000343838.5:n.855+44757T=
ENST00000354728.4:c.855+9345T= (UGT1A9) ENSP00000346768.4:n.855+9345T=
ENST00000373426.3:c.197T= (UGT1A7) ENSP00000362525.3:p.Leu66=
ENST00000373445.1:c.855+44757T= (UGT1A10) ENSP00000362544.1:n.855+44757T=
ENST00000373450.4:c.855+63572T= (UGT1A8) ENSP00000362549.4:n.855+63572T=
NM_019075.2:c.855+44757T= (UGT1A10) NP_061948.1:n.855+44757T=
NM_019076.4:c.855+63572T= (UGT1A8) NP_061949.3:n.855+63572T=
NM_019077.2:c.197T= (UGT1A7) NP_061950.2:p.Leu66=
NM_021027.2:c.855+9345T= (UGT1A9) NP_066307.1:n.855+9345T=
NM_021027.3:c.855+9345T= (UGT1A9) MANE Select NP_066307.1:n.855+9345T=
NM_019075.4:c.855+44757T= (UGT1A10) MANE Select NP_061948.1:n.855+44757T=
NM_019076.5:c.855+63572T= (UGT1A8) MANE Select NP_061949.3:n.855+63572T=
NM_019077.3:c.197T= (UGT1A7) MANE Select NP_061950.2:p.Leu66=