Canonical Allele Identifier: CA2270335328

Gene: PECAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64330939A= , CM000679.2:g.64330939A=	GRCh38
NC_000017.10:g.62408299A= , CM000679.1:g.62408299A=	GRCh37
NC_000017.9:g.59762031A=	NCBI36
NG_047009.1:g.87863T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000442.5:c.2165-1217T= MANE Select	NP_000433.4:n.2165-1217T=
ENST00000563924.6:c.2165-1217T= MANE Select	ENSP00000457421.1:n.2165-1217T=
NM_000442.4:c.2165-1217T=	NP_000433.4:n.2165-1217T=
ENST00000563924.5:c.2165-1217T=	ENSP00000457421.1:n.2165-1217T=
XM_005276880.1:c.2165-7094T=	XP_005276937.1:n.2165-7094T=
XM_005276881.1:c.2108-1217T=	XP_005276938.1:n.2108-1217T=
XM_005276882.1:c.2102-1217T=	XP_005276939.1:n.2102-1217T=
XM_005276883.1:c.2102-7094T=	XP_005276940.1:n.2102-7094T=
XM_005276883.2:c.2102-7094T=	XP_005276940.1:n.2102-7094T=
XM_011524889.1:c.2165-1217T=	XP_011523191.1:n.2165-1217T=
XM_011524889.2:c.2165-1217T=	XP_011523191.1:n.2165-1217T=
XM_011524890.1:c.2165-1217T=	XP_011523192.1:n.2165-1217T=
XM_017024738.1:c.2165-1217T=	XP_016880227.1:n.2165-1217T=
XM_017024739.1:c.2111-1217T=	XP_016880228.1:n.2111-1217T=
XM_017024740.1:c.2108-1217T=	XP_016880229.1:n.2108-1217T=
XM_017024741.1:c.2054-1217T=	XP_016880230.1:n.2054-1217T=