Canonical Allele Identifier: CA2625128922

Gene: SIX1

Linked Data

• gnomAD v4: 14-60649306-C-CTTTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60649310_60649311insATTTG , CM000676.2:g.60649310_60649311insATTTG	GRCh38
NC_000014.8:g.61116028_61116029insATTTG , CM000676.1:g.61116028_61116029insATTTG	GRCh37
NC_000014.7:g.60185781_60185782insATTTG	NCBI36
NG_008231.1:g.5131_5132insTCAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000645694.3:c.-118_-117insTCAAA MANE Select	ENSP00000494686.1:n.-118_-117insTCAAA
ENST00000247182.6:c.-118_-117insTCAAA	ENSP00000247182.5:n.-118_-117insTCAAA
ENST00000553535.2:n.248+2628_248+2629insTCAAA
ENST00000554986.2:c.42-2730_42-2729insTCAAA	ENSP00000452700.2:n.42-2730_42-2729insTCAAA
ENST00000555955.3:n.1197+2628_1197+2629insTCAAA
NM_005982.3:c.-118_-117insTCAAA	NP_005973.1:n.-118_-117insTCAAA
XM_017021602.2:c.-118_-117insTCAAA	XP_016877091.1:n.-118_-117insTCAAA
NM_005982.4:c.-118_-117insTCAAA MANE Select	NP_005973.1:n.-118_-117insTCAAA