Canonical Allele Identifier: CA362378643
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1772690028

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992912G>C , CM000667.2:g.177992912G>C GRCh38
NC_000005.9:g.177419913G>C , CM000667.1:g.177419913G>C GRCh37
NC_000005.8:g.177352519G>C NCBI36
NG_015889.1:g.8331C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.478C>G MANE Select ENSP00000311290.2:p.Pro160Ala
NM_006261.4:c.478C>G NP_006252.3:p.Pro160Ala
NM_006261.5:c.478C>G MANE Select NP_006252.4:p.Pro160Ala