Canonical Allele Identifier: CA387001844

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121857333C>A , CM000674.2:g.121857333C>A GRCh38
NC_000012.11:g.122295239C>A , CM000674.1:g.122295239C>A GRCh37
NC_000012.10:g.120779622C>A NCBI36
NG_016461.1:g.36279G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289004.8:c.193G>T (HPD) MANE Select ENSP00000289004.4:p.Gly65Trp
ENST00000535114.1:n.549G>T (HPD)
ENST00000542159.2:n.251G>T (HPD)
ENST00000543163.5:c.76G>T (HPD) ENSP00000441677.1:p.Gly26Trp
NM_001171993.1:c.76G>T (HPD) NP_001165464.1:p.Gly26Trp
NM_002150.2:c.193G>T (HPD) NP_002141.1:p.Gly65Trp
XR_002957437.1:n.324-286C>A (TIALD)
NM_002150.3:c.193G>T (HPD) MANE Select NP_002141.2:p.Gly65Trp
NM_001171993.2:c.76G>T (HPD) NP_001165464.1:p.Gly26Trp