Canonical Allele Identifier: CA2270343587

Gene: PECAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64350326_64350328delinsCTT , CM000679.2:g.64350326_64350328delinsCTT	GRCh38
NC_000017.9:g.59781431_59781433delinsCTT	NCBI36
NG_047009.1:g.68474_68476delinsAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000563924.6:c.2044+52_2044+54delinsAAG MANE Select	ENSP00000457421.1:n.2044+52_2044+54delinsAAG
ENST00000563924.5:c.2044+52_2044+54delinsAAG	ENSP00000457421.1:n.2044+52_2044+54delinsAAG
NM_000442.4:c.2044+52_2044+54delinsAAG	NP_000433.4:n.2044+52_2044+54delinsAAG
XM_005276880.1:c.2044+52_2044+54delinsAAG	XP_005276937.1:n.2044+52_2044+54delinsAAG
XM_005276881.1:c.2044+52_2044+54delinsAAG	XP_005276938.1:n.2044+52_2044+54delinsAAG
XM_005276882.1:c.2044+52_2044+54delinsAAG	XP_005276939.1:n.2044+52_2044+54delinsAAG
XM_005276883.1:c.2044+52_2044+54delinsAAG	XP_005276940.1:n.2044+52_2044+54delinsAAG
XM_011524889.1:c.2044+52_2044+54delinsAAG	XP_011523191.1:n.2044+52_2044+54delinsAAG
XM_011524890.1:c.2044+52_2044+54delinsAAG	XP_011523192.1:n.2044+52_2044+54delinsAAG
XM_005276883.2:c.2044+52_2044+54delinsAAG	XP_005276940.1:n.2044+52_2044+54delinsAAG
XM_011524889.2:c.2044+52_2044+54delinsAAG	XP_011523191.1:n.2044+52_2044+54delinsAAG
XM_017024738.1:c.2044+52_2044+54delinsAAG	XP_016880227.1:n.2044+52_2044+54delinsAAG
XM_017024739.1:c.1991-2006_1991-2004delinsAAG	XP_016880228.1:n.1991-2006_1991-2004delinsAAG
XM_017024740.1:c.2044+52_2044+54delinsAAG	XP_016880229.1:n.2044+52_2044+54delinsAAG
XM_017024741.1:c.1991-2006_1991-2004delinsAAG	XP_016880230.1:n.1991-2006_1991-2004delinsAAG
NM_000442.5:c.2044+52_2044+54delinsAAG MANE Select	NP_000433.4:n.2044+52_2044+54delinsAAG