Canonical Allele Identifier: CA2671754760

Gene: EGF

Linked Data

• gnomAD v4: 4-109981083-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109981086_109981088del , CM000666.2:g.109981086_109981088del	GRCh38
NC_000004.11:g.110902242_110902244del , CM000666.1:g.110902242_110902244del	GRCh37
NC_000004.10:g.111121691_111121693del	NCBI36
NG_011441.1:g.73203_73205del
NG_011441.2:g.73203_73205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.2371+111_2371+113del MANE Select	ENSP00000265171.5:n.2371+111_2371+113del
ENST00000652245.1:c.2245+111_2245+113del	ENSP00000498337.1:n.2245+111_2245+113del
ENST00000265171.9:c.2371+111_2371+113del	ENSP00000265171.5:n.2371+111_2371+113del
ENST00000503392.1:c.2371+111_2371+113del	ENSP00000421384.1:n.2371+111_2371+113del
ENST00000509793.5:c.2245+111_2245+113del	ENSP00000424316.1:n.2245+111_2245+113del
ENST00000509996.1:n.299+111_299+113del
ENST00000511228.5:n.335+111_335+113del
NM_001178130.1:c.2371+111_2371+113del	NP_001171601.1:n.2371+111_2371+113del
NM_001178131.1:c.2245+111_2245+113del	NP_001171602.1:n.2245+111_2245+113del
NM_001963.4:c.2371+111_2371+113del	NP_001954.2:n.2371+111_2371+113del
XM_005262796.2:c.2371+111_2371+113del	XP_005262853.1:n.2371+111_2371+113del
XM_005262797.2:c.2245+111_2245+113del	XP_005262854.1:n.2245+111_2245+113del
XM_005262798.2:c.2371+111_2371+113del	XP_005262855.1:n.2371+111_2371+113del
XM_005262800.2:c.2371+111_2371+113del	XP_005262857.1:n.2371+111_2371+113del
XM_005262801.2:c.2371+111_2371+113del	XP_005262858.1:n.2371+111_2371+113del
XM_006714124.2:c.2371+111_2371+113del	XP_006714187.1:n.2371+111_2371+113del
XM_011531707.1:c.2260+111_2260+113del	XP_011530009.1:n.2260+111_2260+113del
XM_011531708.1:c.2371+111_2371+113del	XP_011530010.1:n.2371+111_2371+113del
XR_427532.2:n.2824+111_2824+113del
XR_938699.1:n.2824+111_2824+113del
NM_001178130.2:c.2371+111_2371+113del	NP_001171601.1:n.2371+111_2371+113del
NM_001178131.2:c.2245+111_2245+113del	NP_001171602.1:n.2245+111_2245+113del
NM_001357021.1:c.2245+111_2245+113del	NP_001343950.1:n.2245+111_2245+113del
NM_001963.5:c.2371+111_2371+113del	NP_001954.2:n.2371+111_2371+113del
XM_017007845.1:c.2395+111_2395+113del	XP_016863334.1:n.2395+111_2395+113del
XM_017007846.1:c.2395+111_2395+113del	XP_016863335.1:n.2395+111_2395+113del
XM_017007847.1:c.2395+111_2395+113del	XP_016863336.1:n.2395+111_2395+113del
XM_017007848.1:c.2269+111_2269+113del	XP_016863337.1:n.2269+111_2269+113del
XM_017007849.1:c.2395+111_2395+113del	XP_016863338.1:n.2395+111_2395+113del
XM_017007850.1:c.2395+111_2395+113del	XP_016863339.1:n.2395+111_2395+113del
XM_017007851.1:c.2395+111_2395+113del	XP_016863340.1:n.2395+111_2395+113del
XM_017007853.1:c.2395+111_2395+113del	XP_016863342.1:n.2395+111_2395+113del
XR_001741156.1:n.2848+111_2848+113del
XR_001741157.1:n.2848+111_2848+113del
NM_001178130.3:c.2371+111_2371+113del	NP_001171601.1:n.2371+111_2371+113del
NM_001178131.3:c.2245+111_2245+113del	NP_001171602.1:n.2245+111_2245+113del
NM_001357021.2:c.2245+111_2245+113del	NP_001343950.1:n.2245+111_2245+113del
NM_001963.6:c.2371+111_2371+113del MANE Select	NP_001954.2:n.2371+111_2371+113del