Canonical Allele Identifier: CA2543033805

Gene: NECTIN3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111122530_111122531insTCTCTTTCG , CM000665.2:g.111122530_111122531insTCTCTTTCG	GRCh38
NC_000003.11:g.110841377_110841378insTCTCTTTCG , CM000665.1:g.110841377_110841378insTCTCTTTCG	GRCh37
NC_000003.10:g.112324067_112324068insTCTCTTTCG	NCBI36
NG_029835.1:g.55772_55773insTCTCTTTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485303.6:c.917+292_917+293insTCTCTTTCG MANE Select	ENSP00000418070.1:n.917+292_917+293insTCTCTTTCG
ENST00000319792.7:c.917+292_917+293insTCTCTTTCG	ENSP00000321514.3:n.917+292_917+293insTCTCTTTCG
ENST00000485303.5:c.917+292_917+293insTCTCTTTCG	ENSP00000418070.1:n.917+292_917+293insTCTCTTTCG
ENST00000486596.5:c.618+292_618+293insTCTCTTTCG
ENST00000493615.5:c.848+292_848+293insTCTCTTTCG	ENSP00000420579.1:n.848+292_848+293insTCTCTTTCG
NM_001243286.1:c.917+292_917+293insTCTCTTTCG	NP_001230215.1:n.917+292_917+293insTCTCTTTCG
NM_001243288.1:c.848+292_848+293insTCTCTTTCG	NP_001230217.1:n.848+292_848+293insTCTCTTTCG
NM_015480.2:c.917+292_917+293insTCTCTTTCG	NP_056295.1:n.917+292_917+293insTCTCTTTCG
XM_005247322.3:c.917+292_917+293insTCTCTTTCG	XP_005247379.2:n.917+292_917+293insTCTCTTTCG
XM_011512662.1:c.1010+292_1010+293insTCTCTTTCG	XP_011510964.1:n.1010+292_1010+293insTCTCTTTCG
XM_011512663.1:c.1010+292_1010+293insTCTCTTTCG	XP_011510965.1:n.1010+292_1010+293insTCTCTTTCG
XM_011512664.1:c.848+292_848+293insTCTCTTTCG	XP_011510966.1:n.848+292_848+293insTCTCTTTCG
XM_011512665.1:c.1010+292_1010+293insTCTCTTTCG	XP_011510967.1:n.1010+292_1010+293insTCTCTTTCG
XM_011512666.1:c.1010+292_1010+293insTCTCTTTCG	XP_011510968.1:n.1010+292_1010+293insTCTCTTTCG
XM_011512667.1:c.281+292_281+293insTCTCTTTCG	XP_011510969.1:n.281+292_281+293insTCTCTTTCG
XR_924122.1:n.1240+292_1240+293insTCTCTTTCG
XM_017006123.1:c.1010+292_1010+293insTCTCTTTCG	XP_016861612.1:n.1010+292_1010+293insTCTCTTTCG
XM_017006124.1:c.872+292_872+293insTCTCTTTCG	XP_016861613.1:n.872+292_872+293insTCTCTTTCG
XM_017006125.1:c.848+292_848+293insTCTCTTTCG	XP_016861614.1:n.848+292_848+293insTCTCTTTCG
XM_017006126.1:c.917+292_917+293insTCTCTTTCG	XP_016861615.1:n.917+292_917+293insTCTCTTTCG
XM_017006127.2:c.281+292_281+293insTCTCTTTCG	XP_016861616.1:n.281+292_281+293insTCTCTTTCG
XR_002959508.1:n.1198+292_1198+293insTCTCTTTCG
XR_924122.2:n.1240+292_1240+293insTCTCTTTCG
NM_015480.3:c.917+292_917+293insTCTCTTTCG MANE Select	NP_056295.1:n.917+292_917+293insTCTCTTTCG
NM_001243286.2:c.917+292_917+293insTCTCTTTCG	NP_001230215.1:n.917+292_917+293insTCTCTTTCG
NM_001243288.2:c.848+292_848+293insTCTCTTTCG	NP_001230217.1:n.848+292_848+293insTCTCTTTCG