Canonical Allele Identifier: CA2426745208

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949735T= , CM000685.2:g.43949735T= GRCh38
NC_000023.10:g.43808981T= , CM000685.1:g.43808981T= GRCh37
NC_000023.9:g.43693925T= NCBI36
NG_009832.1:g.28941A=

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*64A= (NDP) MANE Select ENSP00000495972.1:n.*64A=
ENST00000647044.1:c.*64A= (NDP) ENSP00000495811.1:n.*64A=
ENST00000378062.5:c.*64A= (NDP) ENSP00000367301.5:n.*64A=
ENST00000470584.1:n.510A= (NDP)
NM_000266.3:c.*64A= (NDP) NP_000257.1:n.*64A=
NR_046631.1:n.4T= (NDP-AS1)
NM_000266.4:c.*64A= (NDP) MANE Select NP_000257.1:n.*64A=