Canonical Allele Identifier: CA1327642310

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216028947G= , CM000664.2:g.216028947G= GRCh38
NC_000002.11:g.216893670G= , CM000664.1:g.216893670G= GRCh37
NC_000002.10:g.216601915G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000420348.1:c.-68+3842C= (MREG) ENSP00000404470.1:n.-68+3842C=
ENST00000424992.5:c.-68+5015C= (MREG) ENSP00000413302.1:n.-68+5015C=
ENST00000439791.5:c.-68+4736C= (MREG) ENSP00000411076.1:n.-68+4736C=
ENST00000442122.5:c.*440+10244C= (PECR) ENSP00000395512.1:n.*440+10244C=
NM_001372189.1:c.-68+5015C= (MREG) NP_001359118.1:n.-68+5015C=
NM_001372190.1:c.-68+4736C= (MREG) NP_001359119.1:n.-68+4736C=