Canonical Allele Identifier: CA2639345994
Gene: PECAM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.64350318C>A , CM000679.2:g.64350318C>A GRCh38
NC_000017.9:g.59781423C>A NCBI36
NG_047009.1:g.68484G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000563924.6:c.2044+62G>T MANE Select ENSP00000457421.1:n.2044+62G>T
ENST00000563924.5:c.2044+62G>T ENSP00000457421.1:n.2044+62G>T
NM_000442.4:c.2044+62G>T NP_000433.4:n.2044+62G>T
XM_005276880.1:c.2044+62G>T XP_005276937.1:n.2044+62G>T
XM_005276881.1:c.2044+62G>T XP_005276938.1:n.2044+62G>T
XM_005276882.1:c.2044+62G>T XP_005276939.1:n.2044+62G>T
XM_005276883.1:c.2044+62G>T XP_005276940.1:n.2044+62G>T
XM_011524889.1:c.2044+62G>T XP_011523191.1:n.2044+62G>T
XM_011524890.1:c.2044+62G>T XP_011523192.1:n.2044+62G>T
XM_005276883.2:c.2044+62G>T XP_005276940.1:n.2044+62G>T
XM_011524889.2:c.2044+62G>T XP_011523191.1:n.2044+62G>T
XM_017024738.1:c.2044+62G>T XP_016880227.1:n.2044+62G>T
XM_017024739.1:c.1991-1996G>T XP_016880228.1:n.1991-1996G>T
XM_017024740.1:c.2044+62G>T XP_016880229.1:n.2044+62G>T
XM_017024741.1:c.1991-1996G>T XP_016880230.1:n.1991-1996G>T
NM_000442.5:c.2044+62G>T MANE Select NP_000433.4:n.2044+62G>T