Canonical Allele Identifier: CA2526364

Gene: CD47

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.108080136T>A , CM000665.2:g.108080136T>A	GRCh38
NC_000003.11:g.107798983T>A , CM000665.1:g.107798983T>A	GRCh37
NC_000003.10:g.109281673T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355354.13:c.255A>T	ENSP00000347512.7:p.Lys85Asn
ENST00000361309.6:c.255A>T MANE Select	ENSP00000355361.5:p.Lys85Asn
ENST00000644850.1:c.120A>T	ENSP00000493750.1:p.Lys40Asn
ENST00000355354.11:c.255A>T	ENSP00000347512.7:p.Lys85Asn
ENST00000361309.5:c.255A>T	ENSP00000355361.5:p.Lys85Asn
NM_001777.3:c.255A>T	NP_001768.1:p.Lys85Asn
NM_198793.2:c.255A>T	NP_942088.1:p.Lys85Asn
XM_005247908.1:c.255A>T	XP_005247965.1:p.Lys85Asn
XM_005247909.1:c.255A>T	XP_005247966.1:p.Lys85Asn
XR_241521.1:n.405A>T
XR_241522.1:n.405A>T
XR_924218.1:n.405A>T
XR_924219.1:n.405A>T
XR_924220.1:n.405A>T
XM_005247908.2:c.255A>T	XP_005247965.1:p.Lys85Asn
XM_005247909.2:c.255A>T	XP_005247966.1:p.Lys85Asn
XR_001740374.2:n.392A>T
XR_001740375.2:n.392A>T
XR_002959610.1:n.392A>T
XR_002959611.1:n.392A>T
XR_241521.2:n.392A>T
XR_241522.2:n.392A>T
XR_924218.2:n.392A>T
XR_924219.2:n.392A>T
XR_924220.2:n.392A>T
NM_001382306.1:c.255A>T	NP_001369235.1:p.Lys85Asn
NM_001777.4:c.255A>T MANE Select	NP_001768.1:p.Lys85Asn
NM_198793.3:c.255A>T	NP_942088.1:p.Lys85Asn