Canonical Allele Identifier: CA357874626

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925698T>A (hg19) ; chr4:g.110004542T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004542T>A , CM000666.2:g.110004542T>A	GRCh38
NC_000004.11:g.110925698T>A , CM000666.1:g.110925698T>A	GRCh37
NC_000004.10:g.111145147T>A	NCBI36
NG_011441.1:g.96659T>A
NG_011441.2:g.96659T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.3211T>A MANE Select	ENSP00000265171.5:p.Tyr1071Asn
ENST00000652245.1:c.2842T>A	ENSP00000498337.1:p.Tyr948Asn
ENST00000265171.9:c.3211T>A	ENSP00000265171.5:p.Tyr1071Asn
ENST00000503392.1:c.3088T>A	ENSP00000421384.1:p.Tyr1030Asn
ENST00000509793.5:c.3085T>A	ENSP00000424316.1:p.Tyr1029Asn
ENST00000509996.1:n.896T>A
ENST00000537316.5:n.42T>A
ENST00000540840.1:n.42T>A
ENST00000544918.1:n.296T>A
NM_001178130.1:c.3088T>A	NP_001171601.1:p.Tyr1030Asn
NM_001178131.1:c.3085T>A	NP_001171602.1:p.Tyr1029Asn
NM_001963.4:c.3211T>A	NP_001954.2:p.Tyr1071Asn
XM_005262796.2:c.3211T>A	XP_005262853.1:p.Tyr1071Asn
XM_005262797.2:c.3085T>A	XP_005262854.1:p.Tyr1029Asn
XM_005262798.2:c.2968T>A	XP_005262855.1:p.Tyr990Asn
XM_005262800.2:c.2968T>A	XP_005262857.1:p.Tyr990Asn
XM_005262801.2:c.2492-6660T>A	XP_005262858.1:n.2492-6660T>A
XM_006714124.2:c.3211T>A	XP_006714187.1:p.Tyr1071Asn
XM_011531707.1:c.3100T>A	XP_011530009.1:p.Tyr1034Asn
XR_427532.2:n.3225T>A
XR_938699.1:n.3225T>A
NM_001178130.2:c.3088T>A	NP_001171601.1:p.Tyr1030Asn
NM_001178131.2:c.3085T>A	NP_001171602.1:p.Tyr1029Asn
NM_001357021.1:c.2842T>A	NP_001343950.1:p.Tyr948Asn
NM_001963.5:c.3211T>A	NP_001954.2:p.Tyr1071Asn
XM_017007845.1:c.3235T>A	XP_016863334.1:p.Tyr1079Asn
XM_017007846.1:c.3235T>A	XP_016863335.1:p.Tyr1079Asn
XM_017007847.1:c.3112T>A	XP_016863336.1:p.Tyr1038Asn
XM_017007848.1:c.3109T>A	XP_016863337.1:p.Tyr1037Asn
XM_017007849.1:c.2992T>A	XP_016863338.1:p.Tyr998Asn
XM_017007850.1:c.3235T>A	XP_016863339.1:p.Tyr1079Asn
XM_017007851.1:c.2992T>A	XP_016863340.1:p.Tyr998Asn
XR_001741156.1:n.3249T>A
XR_001741157.1:n.3249T>A
NM_001178130.3:c.3088T>A	NP_001171601.1:p.Tyr1030Asn
NM_001178131.3:c.3085T>A	NP_001171602.1:p.Tyr1029Asn
NM_001357021.2:c.2842T>A	NP_001343950.1:p.Tyr948Asn
NM_001963.6:c.3211T>A MANE Select	NP_001954.2:p.Tyr1071Asn