Canonical Allele Identifier: CA359590722

Gene: C7

Linked Data

• COSMIC: COSM3616463
• MyVariant Identifiers: chr5:g.40964859T>A (hg19) ; chr5:g.40964757T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964757T>A , CM000667.2:g.40964757T>A	GRCh38
NC_000005.9:g.40964859T>A , CM000667.1:g.40964859T>A	GRCh37
NC_000005.8:g.41000616T>A	NCBI36
NG_011692.1:g.60261T>A , LRG_30:g.60261T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.558T>A
ENST00000696333.1:c.1766T>A	ENSP00000512566.1:p.Phe589Tyr
ENST00000696441.1:c.1766T>A	ENSP00000512631.1:p.Phe589Tyr
ENST00000706664.1:n.1880T>A
ENST00000706666.1:n.1842T>A
ENST00000706667.1:n.2656T>A
ENST00000706668.1:n.2494T>A
ENST00000313164.10:c.1766T>A MANE Select	ENSP00000322061.9:p.Phe589Tyr
ENST00000313164.9:c.1766T>A	ENSP00000322061.9:p.Phe589Tyr
ENST00000486779.1:n.279T>A
NM_000587.2:c.1766T>A , LRG_30t1:c.1766T>A	NP_000578.2:p.Phe589Tyr
XM_011514122.1:c.1766T>A	XP_011512424.1:p.Phe589Tyr
NM_000587.3:c.1766T>A	NP_000578.2:p.Phe589Tyr
NM_000587.4:c.1766T>A MANE Select	NP_000578.2:p.Phe589Tyr