Canonical Allele Identifier: CA362378591

Gene: PROP1

Linked Data

• MyVariant Identifiers: chr5:g.177419886G>C (hg19) ; chr5:g.177992885G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177992885G>C , CM000667.2:g.177992885G>C	GRCh38
NC_000005.9:g.177419886G>C , CM000667.1:g.177419886G>C	GRCh37
NC_000005.8:g.177352492G>C	NCBI36
NG_015889.1:g.8358C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.505C>G MANE Select	ENSP00000311290.2:p.His169Asp
NM_006261.4:c.505C>G	NP_006252.3:p.His169Asp
NM_006261.5:c.505C>G MANE Select	NP_006252.4:p.His169Asp