Canonical Allele Identifier: CA1867772680

Gene: INVS

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.100240073_100240075delinsCAG , CM000671.2:g.100240073_100240075delinsCAG	GRCh38
NC_000009.11:g.103002355_103002357delinsCAG , CM000671.1:g.103002355_103002357delinsCAG	GRCh37
NC_000009.10:g.102042176_102042178delinsCAG	NCBI36
NG_008316.1:g.145845_145847delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000262457.7:c.629_631delinsCAG MANE Select	ENSP00000262457.2:p.Thr210=
ENST00000262456.6:c.629_631delinsCAG	ENSP00000262456.2:p.Thr210=
ENST00000262457.6:c.629_631delinsCAG	ENSP00000262457.2:p.Thr210=
ENST00000460636.2:n.901_903delinsCAG
NM_014425.3:c.629_631delinsCAG	NP_055240.2:p.Thr210=
NM_183245.2:c.629_631delinsCAG	NP_899068.1:p.Thr210=
NR_051962.1:n.938_940delinsCAG
XM_005251923.3:c.629_631delinsCAG	XP_005251980.1:p.Thr210=
XM_005251924.3:c.341_343delinsCAG	XP_005251981.1:p.Thr114=
XM_011518531.1:c.629_631delinsCAG	XP_011516833.1:p.Thr210=
XM_011518532.1:c.629_631delinsCAG	XP_011516834.1:p.Thr210=
XM_011518533.1:c.629_631delinsCAG	XP_011516835.1:p.Thr210=
XM_011518534.1:c.341_343delinsCAG	XP_011516836.1:p.Thr114=
XM_011518535.1:c.341_343delinsCAG	XP_011516837.1:p.Thr114=
XM_011518536.1:c.341_343delinsCAG	XP_011516838.1:p.Thr114=
XM_011518537.1:c.341_343delinsCAG	XP_011516839.1:p.Thr114=
XM_011518538.1:c.341_343delinsCAG	XP_011516840.1:p.Thr114=
XM_011518539.1:c.308_310delinsCAG	XP_011516841.1:p.Thr103=
XM_011518540.1:c.308_310delinsCAG	XP_011516842.1:p.Thr103=
XM_011518541.1:c.308_310delinsCAG	XP_011516843.1:p.Thr103=
XM_011518542.1:c.341_343delinsCAG	XP_011516844.1:p.Thr114=
XM_011518543.1:c.-361_-359delinsCAG	XP_011516845.1:n.-361_-359delinsCAG
XR_242585.1:n.885_887delinsCAG
XR_242586.1:n.885_887delinsCAG
XR_428522.1:n.885_887delinsCAG
NM_001318381.1:c.341_343delinsCAG	NP_001305310.1:p.Thr114=
NM_001318382.1:c.-361_-359delinsCAG	NP_001305311.1:n.-361_-359delinsCAG
NM_014425.4:c.629_631delinsCAG	NP_055240.2:p.Thr210=
NR_134606.1:n.885_887delinsCAG
NM_014425.5:c.629_631delinsCAG MANE Select	NP_055240.2:p.Thr210=
NM_001318381.2:c.341_343delinsCAG	NP_001305310.1:p.Thr114=
NM_001318382.2:c.-361_-359delinsCAG	NP_001305311.1:n.-361_-359delinsCAG
NR_134606.2:n.827_829delinsCAG