Canonical Allele Identifier: CA1630962

Linked Data

dbSNP Id: rs371208214
gnomAD v2: 2-42996926-C-T
gnomAD v3: 2-42769786-C-T
gnomAD v4: 2-42769786-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.42769786C>T , CM000664.2:g.42769786C>T GRCh38
NC_000002.11:g.42996926C>T , CM000664.1:g.42996926C>T GRCh37
NC_000002.10:g.42850430C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000294973.11:c.557G>A (HAAO) MANE Select ENSP00000294973.6:p.Trp186Ter
ENST00000294973.10:c.557G>A (HAAO) ENSP00000294973.6:p.Trp186Ter
ENST00000402698.6:n.901G>A (HAAO)
ENST00000404451.7:n.389+357G>A (HAAO)
ENST00000406007.6:n.108G>A (HAAO)
ENST00000431905.1:c.455G>A (HAAO) ENSP00000412601.1:p.Trp152Ter
NM_012205.2:c.557G>A (HAAO) NP_036337.2:p.Trp186Ter
XM_005264230.2:c.484+357G>A (HAAO) XP_005264287.1:n.484+357G>A
XM_011532729.1:c.467G>A (HAAO) XP_011531031.1:p.Trp156Ter
XM_011532730.1:c.455G>A (HAAO) XP_011531032.1:p.Trp152Ter
XM_011532731.1:c.394+357G>A (HAAO) XP_011531033.1:n.394+357G>A
XR_939697.1:n.1791-14129C>T (MTA3)
XM_005264230.4:c.484+357G>A (HAAO) XP_005264287.1:n.484+357G>A
XM_011532729.3:c.467G>A (HAAO) XP_011531031.1:p.Trp156Ter
XM_011532730.3:c.455G>A (HAAO) XP_011531032.1:p.Trp152Ter
XM_011532731.3:c.394+357G>A (HAAO) XP_011531033.1:n.394+357G>A
XM_017003717.2:c.382+357G>A (HAAO) XP_016859206.1:n.382+357G>A
XM_024452774.1:c.484+357G>A (HAAO) XP_024308542.1:n.484+357G>A
XM_024452775.1:c.382+357G>A (HAAO) XP_024308543.1:n.382+357G>A
XR_001738859.2:n.1794-14129C>T (MTA3)
XR_939697.3:n.1794-14129C>T (MTA3)
NM_012205.3:c.557G>A (HAAO) MANE Select NP_036337.2:p.Trp186Ter