Canonical Allele Identifier: CA2625696123

Gene: PROX2 YLPM1

Linked Data

• gnomAD v4: 14-74855014-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74855014A>T , CM000676.2:g.74855014A>T	GRCh38
NC_000014.8:g.75321717A>T , CM000676.1:g.75321717A>T	GRCh37
NC_000014.7:g.74391470A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556489.4:c.*118T>A (PROX2) MANE Select	ENSP00000451223.2:n.*118T>A
ENST00000673765.1:c.*118T>A (PROX2)	ENSP00000501015.1:n.*118T>A
ENST00000553381.1:n.238-203A>T (YLPM1)
ENST00000554107.2:c.206-203A>T (YLPM1)
ENST00000556084.6:c.1216T>A (PROX2)	ENSP00000451463.2:n.1216T>A
ENST00000556489.3:c.1897T>A (PROX2)	ENSP00000451223.2:n.1897T>A
NM_001080408.2:c.1216T>A (PROX2)	NP_001073877.2:n.1216T>A
NM_001243007.1:c.1897T>A (PROX2)	NP_001229936.1:n.1897T>A
XM_005267543.2:c.*118T>A (PROX2)	XP_005267600.1:n.*118T>A
NM_001080408.3:c.*118T>A (PROX2)	NP_001073877.2:n.*118T>A
NM_001243007.2:c.*118T>A (PROX2) MANE Select	NP_001229936.1:n.*118T>A
NM_001384314.1:c.*118T>A (PROX2)	NP_001371243.1:n.*118T>A
NR_169190.1:n.2522T>A (PROX2)