Canonical Allele Identifier: CA357884952

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110902024T>C (hg19) ; chr4:g.109980868T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109980868T>C , CM000666.2:g.109980868T>C	GRCh38
NC_000004.11:g.110902024T>C , CM000666.1:g.110902024T>C	GRCh37
NC_000004.10:g.111121473T>C	NCBI36
NG_011441.1:g.72985T>C
NG_011441.2:g.72985T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.2264T>C MANE Select	ENSP00000265171.5:p.Ile755Thr
ENST00000652245.1:c.2138T>C	ENSP00000498337.1:p.Ile713Thr
ENST00000265171.9:c.2264T>C	ENSP00000265171.5:p.Ile755Thr
ENST00000503392.1:c.2264T>C	ENSP00000421384.1:p.Ile755Thr
ENST00000509793.5:c.2138T>C	ENSP00000424316.1:p.Ile713Thr
ENST00000509996.1:n.192T>C
ENST00000511228.5:n.228T>C
NM_001178130.1:c.2264T>C	NP_001171601.1:p.Ile755Thr
NM_001178131.1:c.2138T>C	NP_001171602.1:p.Ile713Thr
NM_001963.4:c.2264T>C	NP_001954.2:p.Ile755Thr
XM_005262796.2:c.2264T>C	XP_005262853.1:p.Ile755Thr
XM_005262797.2:c.2138T>C	XP_005262854.1:p.Ile713Thr
XM_005262798.2:c.2264T>C	XP_005262855.1:p.Ile755Thr
XM_005262800.2:c.2264T>C	XP_005262857.1:p.Ile755Thr
XM_005262801.2:c.2264T>C	XP_005262858.1:p.Ile755Thr
XM_006714124.2:c.2264T>C	XP_006714187.1:p.Ile755Thr
XM_011531707.1:c.2153T>C	XP_011530009.1:p.Ile718Thr
XM_011531708.1:c.2264T>C	XP_011530010.1:p.Ile755Thr
XR_427532.2:n.2717T>C
XR_938699.1:n.2717T>C
NM_001178130.2:c.2264T>C	NP_001171601.1:p.Ile755Thr
NM_001178131.2:c.2138T>C	NP_001171602.1:p.Ile713Thr
NM_001357021.1:c.2138T>C	NP_001343950.1:p.Ile713Thr
NM_001963.5:c.2264T>C	NP_001954.2:p.Ile755Thr
XM_017007845.1:c.2288T>C	XP_016863334.1:p.Ile763Thr
XM_017007846.1:c.2288T>C	XP_016863335.1:p.Ile763Thr
XM_017007847.1:c.2288T>C	XP_016863336.1:p.Ile763Thr
XM_017007848.1:c.2162T>C	XP_016863337.1:p.Ile721Thr
XM_017007849.1:c.2288T>C	XP_016863338.1:p.Ile763Thr
XM_017007850.1:c.2288T>C	XP_016863339.1:p.Ile763Thr
XM_017007851.1:c.2288T>C	XP_016863340.1:p.Ile763Thr
XM_017007853.1:c.2288T>C	XP_016863342.1:p.Ile763Thr
XR_001741156.1:n.2741T>C
XR_001741157.1:n.2741T>C
NM_001178130.3:c.2264T>C	NP_001171601.1:p.Ile755Thr
NM_001178131.3:c.2138T>C	NP_001171602.1:p.Ile713Thr
NM_001357021.2:c.2138T>C	NP_001343950.1:p.Ile713Thr
NM_001963.6:c.2264T>C MANE Select	NP_001954.2:p.Ile755Thr