Canonical Allele Identifier: CA419396921

Linked Data

MyVariant Identifiers: chr1:g.110604078G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110061456G>A , CM000663.2:g.110061456G>A GRCh38
NC_000001.10:g.110604078G>A , CM000663.1:g.110604078G>A GRCh37
NC_000001.9:g.110405601G>A NCBI36
NG_012039.1:g.14245C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.702C>T (ALX3) MANE Select ENSP00000497310.1:p.Pro234=
ENST00000649954.1:c.273C>T (ALX3) ENSP00000497035.1:p.Pro91=
ENST00000369792.4:c.702C>T (ALX3) ENSP00000358807.3:p.Pro234=
ENST00000473429.5:n.4213+6654G>A (STRIP1)
NM_006492.2:c.702C>T (ALX3) NP_006483.2:p.Pro234=
NM_006492.3:c.702C>T (ALX3) MANE Select NP_006483.2:p.Pro234=