Canonical Allele Identifier: CA1867772675

Gene: INVS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.100240056T= , CM000671.2:g.100240056T=	GRCh38
NC_000009.11:g.103002338T= , CM000671.1:g.103002338T=	GRCh37
NC_000009.10:g.102042159T=	NCBI36
NG_008316.1:g.145828T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262457.7:c.616-4T= MANE Select	ENSP00000262457.2:n.616-4T=
ENST00000262456.6:c.616-4T=	ENSP00000262456.2:n.616-4T=
ENST00000262457.6:c.616-4T=	ENSP00000262457.2:n.616-4T=
ENST00000460636.2:n.888-4T=
NM_014425.3:c.616-4T=	NP_055240.2:n.616-4T=
NM_183245.2:c.616-4T=	NP_899068.1:n.616-4T=
NR_051962.1:n.925-4T=
XM_005251923.3:c.616-4T=	XP_005251980.1:n.616-4T=
XM_005251924.3:c.328-4T=	XP_005251981.1:n.328-4T=
XM_011518531.1:c.616-4T=	XP_011516833.1:n.616-4T=
XM_011518532.1:c.616-4T=	XP_011516834.1:n.616-4T=
XM_011518533.1:c.616-4T=	XP_011516835.1:n.616-4T=
XM_011518534.1:c.328-4T=	XP_011516836.1:n.328-4T=
XM_011518535.1:c.328-4T=	XP_011516837.1:n.328-4T=
XM_011518536.1:c.328-4T=	XP_011516838.1:n.328-4T=
XM_011518537.1:c.328-4T=	XP_011516839.1:n.328-4T=
XM_011518538.1:c.328-4T=	XP_011516840.1:n.328-4T=
XM_011518539.1:c.295-4T=	XP_011516841.1:n.295-4T=
XM_011518540.1:c.295-4T=	XP_011516842.1:n.295-4T=
XM_011518541.1:c.295-4T=	XP_011516843.1:n.295-4T=
XM_011518542.1:c.328-4T=	XP_011516844.1:n.328-4T=
XM_011518543.1:c.-374-4T=	XP_011516845.1:n.-374-4T=
XR_242585.1:n.872-4T=
XR_242586.1:n.872-4T=
XR_428522.1:n.872-4T=
NM_001318381.1:c.328-4T=	NP_001305310.1:n.328-4T=
NM_001318382.1:c.-374-4T=	NP_001305311.1:n.-374-4T=
NM_014425.4:c.616-4T=	NP_055240.2:n.616-4T=
NR_134606.1:n.872-4T=
NM_014425.5:c.616-4T= MANE Select	NP_055240.2:n.616-4T=
NM_001318381.2:c.328-4T=	NP_001305310.1:n.328-4T=
NM_001318382.2:c.-374-4T=	NP_001305311.1:n.-374-4T=
NR_134606.2:n.814-4T=