Canonical Allele Identifier: CA2147230618

Gene: PROX2 YLPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74855022G= , CM000676.2:g.74855022G=	GRCh38
NC_000014.8:g.75321725G= , CM000676.1:g.75321725G=	GRCh37
NC_000014.7:g.74391478G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556489.4:c.*110C= (PROX2) MANE Select	ENSP00000451223.2:n.*110C=
ENST00000673765.1:c.*110C= (PROX2)	ENSP00000501015.1:n.*110C=
ENST00000553381.1:n.238-195G= (YLPM1)
ENST00000554107.2:c.206-195G= (YLPM1)
ENST00000556084.6:c.1208C= (PROX2)	ENSP00000451463.2:n.1208C=
ENST00000556489.3:c.1889C= (PROX2)	ENSP00000451223.2:n.1889C=
NM_001080408.2:c.1208C= (PROX2)	NP_001073877.2:n.1208C=
NM_001243007.1:c.1889C= (PROX2)	NP_001229936.1:n.1889C=
XM_005267543.2:c.*110C= (PROX2)	XP_005267600.1:n.*110C=
NM_001080408.3:c.*110C= (PROX2)	NP_001073877.2:n.*110C=
NM_001243007.2:c.*110C= (PROX2) MANE Select	NP_001229936.1:n.*110C=
NM_001384314.1:c.*110C= (PROX2)	NP_001371243.1:n.*110C=
NR_169190.1:n.2514C= (PROX2)