Canonical Allele Identifier: CA2676773953
Gene: PROP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992546dup , CM000667.2:g.177992546dup GRCh38
NC_000005.9:g.177419547dup , CM000667.1:g.177419547dup GRCh37
NC_000005.8:g.177352153dup NCBI36
NG_015889.1:g.8700dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*166dup MANE Select ENSP00000311290.2:n.*166dup
NM_006261.4:c.*166dup NP_006252.3:n.*166dup
NM_006261.5:c.*166dup MANE Select NP_006252.4:n.*166dup