Canonical Allele Identifier: CA2147233242

Gene: PROX2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74860740T>A , CM000676.2:g.74860740T>A	GRCh38
NC_000014.8:g.75327443T>A , CM000676.1:g.75327443T>A	GRCh37
NC_000014.7:g.74397196T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556489.4:c.1305+1790A>T MANE Select	ENSP00000451223.2:n.1305+1790A>T
ENST00000673765.1:c.732+2363A>T	ENSP00000501015.1:n.732+2363A>T
ENST00000556084.6:c.732+2363A>T	ENSP00000451463.2:n.732+2363A>T
ENST00000556489.3:c.1305+1790A>T	ENSP00000451223.2:n.1305+1790A>T
NM_001080408.2:c.732+2363A>T	NP_001073877.2:n.732+2363A>T
NM_001243007.1:c.1305+1790A>T	NP_001229936.1:n.1305+1790A>T
XM_005267543.2:c.1311+471A>T	XP_005267600.1:n.1311+471A>T
XM_005267543.4:c.1311+471A>T	XP_005267600.1:n.1311+471A>T
XM_017021222.1:c.*1769A>T	XP_016876711.1:n.*1769A>T
NM_001080408.3:c.732+2363A>T	NP_001073877.2:n.732+2363A>T
NM_001243007.2:c.1305+1790A>T MANE Select	NP_001229936.1:n.1305+1790A>T
NM_001384314.1:c.1305+1790A>T	NP_001371243.1:n.1305+1790A>T
NR_169190.1:n.1807+1790A>T