Canonical Allele Identifier: CA2581692622

Gene: PAPPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.176823113A>T , CM000663.2:g.176823113A>T	GRCh38
NC_000001.10:g.176792249A>T , CM000663.1:g.176792249A>T	GRCh37
NC_000001.9:g.175058872A>T	NCBI36
NG_023390.1:g.364943A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367662.5:c.5203-17060A>T MANE Select	ENSP00000356634.3:n.5203-17060A>T
ENST00000367662.4:c.5203-17060A>T	ENSP00000356634.3:n.5203-17060A>T
ENST00000479836.1:n.221-13522A>T
NM_020318.2:c.5203-17060A>T	NP_064714.2:n.5203-17060A>T
XM_005245422.2:c.5203-17060A>T	XP_005245479.1:n.5203-17060A>T
XM_011509857.1:c.5203-17060A>T	XP_011508159.1:n.5203-17060A>T
XM_011509858.1:c.5203-17060A>T	XP_011508160.1:n.5203-17060A>T
XM_011509859.1:c.5288-13522A>T	XP_011508161.1:n.5288-13522A>T
XR_921907.1:n.6452-17060A>T
XM_005245422.3:c.5203-17060A>T	XP_005245479.1:n.5203-17060A>T
XM_011509858.2:c.5203-17060A>T	XP_011508160.1:n.5203-17060A>T
XM_017002023.1:c.5203-17060A>T	XP_016857512.1:n.5203-17060A>T
XM_017002024.1:c.5203-17060A>T	XP_016857513.1:n.5203-17060A>T
XM_017002025.2:c.5203-17060A>T	XP_016857514.1:n.5203-17060A>T
XR_921907.2:n.6464-17060A>T
NM_020318.3:c.5203-17060A>T MANE Select	NP_064714.2:n.5203-17060A>T