Canonical Allele Identifier: CA2426745294

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949972G= , CM000685.2:g.43949972G= GRCh38
NC_000023.10:g.43809218G= , CM000685.1:g.43809218G= GRCh37
NC_000023.9:g.43694162G= NCBI36
NG_009832.1:g.28704C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.229C= (NDP) MANE Select ENSP00000495972.1:p.Pro77=
ENST00000647044.1:c.229C= (NDP) ENSP00000495811.1:p.Pro77=
ENST00000378062.5:c.229C= (NDP) ENSP00000367301.5:p.Pro77=
ENST00000470584.1:n.273C= (NDP)
NM_000266.3:c.229C= (NDP) NP_000257.1:p.Pro77=
NR_046631.1:n.241G= (NDP-AS1)
NM_000266.4:c.229C= (NDP) MANE Select NP_000257.1:p.Pro77=