Canonical Allele Identifier: CA2639346023

Gene: PECAM1

Linked Data

• gnomAD v4: 17-64350357-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64350357A>G , CM000679.2:g.64350357A>G	GRCh38
NC_000017.9:g.59781462A>G	NCBI36
NG_047009.1:g.68445T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000563924.6:c.2044+23T>C MANE Select	ENSP00000457421.1:n.2044+23T>C
ENST00000563924.5:c.2044+23T>C	ENSP00000457421.1:n.2044+23T>C
NM_000442.4:c.2044+23T>C	NP_000433.4:n.2044+23T>C
XM_005276880.1:c.2044+23T>C	XP_005276937.1:n.2044+23T>C
XM_005276881.1:c.2044+23T>C	XP_005276938.1:n.2044+23T>C
XM_005276882.1:c.2044+23T>C	XP_005276939.1:n.2044+23T>C
XM_005276883.1:c.2044+23T>C	XP_005276940.1:n.2044+23T>C
XM_011524889.1:c.2044+23T>C	XP_011523191.1:n.2044+23T>C
XM_011524890.1:c.2044+23T>C	XP_011523192.1:n.2044+23T>C
XM_005276883.2:c.2044+23T>C	XP_005276940.1:n.2044+23T>C
XM_011524889.2:c.2044+23T>C	XP_011523191.1:n.2044+23T>C
XM_017024738.1:c.2044+23T>C	XP_016880227.1:n.2044+23T>C
XM_017024739.1:c.1990+2033T>C	XP_016880228.1:n.1990+2033T>C
XM_017024740.1:c.2044+23T>C	XP_016880229.1:n.2044+23T>C
XM_017024741.1:c.1990+2033T>C	XP_016880230.1:n.1990+2033T>C
NM_000442.5:c.2044+23T>C MANE Select	NP_000433.4:n.2044+23T>C