Canonical Allele Identifier: CA362379058

Gene: PROP1

Linked Data

• gnomAD v4: 5-177994162-T-G
• MyVariant Identifiers: chr5:g.177421163T>G (hg19) ; chr5:g.177994162T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177994162T>G , CM000667.2:g.177994162T>G	GRCh38
NC_000005.9:g.177421163T>G , CM000667.1:g.177421163T>G	GRCh37
NC_000005.8:g.177353769T>G	NCBI36
NG_015889.1:g.7081A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.286A>C MANE Select	ENSP00000311290.2:p.Ile96Leu
NM_006261.4:c.286A>C	NP_006252.3:p.Ile96Leu
NM_006261.5:c.286A>C MANE Select	NP_006252.4:p.Ile96Leu