Canonical Allele Identifier: CA350882445
Community Standard Title: NM_178821.3(DAW1):c.1116G>T (p.Trp372Cys)
Gene: DAW1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227921464G>T , CM000664.2:g.227921464G>T GRCh38
NC_000002.11:g.228786180G>T , CM000664.1:g.228786180G>T GRCh37
NC_000002.10:g.228494424G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_178821.3:c.1116G>T MANE Select NP_849143.1:p.Trp372Cys
ENST00000309931.3:c.1116G>T MANE Select ENSP00000311899.2:p.Trp372Cys
NM_001330004.1:c.1071G>T NP_001316933.1:p.Trp357Cys
NM_001330004.2:c.1071G>T NP_001316933.1:p.Trp357Cys
NM_178821.1:c.1116G>T NP_849143.1:p.Trp372Cys
NM_178821.2:c.1116G>T NP_849143.1:p.Trp372Cys
NR_138459.1:n.1646G>T
NR_138459.2:n.1391G>T
ENST00000309931.2:c.1116G>T ENSP00000311899.2:p.Trp372Cys
ENST00000373666.6:c.*222G>T ENSP00000362770.2:n.*222G>T
XM_011510755.1:c.1071G>T XP_011509057.1:p.Trp357Cys
XM_017003490.1:c.528G>T XP_016858979.1:p.Trp176Cys