Canonical Allele Identifier: CA2687993763

Gene: GDF6

Linked Data

• gnomAD v4: 8-96160175-A-ATTTAAGAAAAGTAAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.96160175_96160176insTTTAAGAAAAGTAAAAG , CM000670.2:g.96160175_96160176insTTTAAGAAAAGTAAAAG	GRCh38
NC_000008.10:g.97172403_97172404insTTTAAGAAAAGTAAAAG , CM000670.1:g.97172403_97172404insTTTAAGAAAAGTAAAAG	GRCh37
NC_000008.9:g.97241579_97241580insTTTAAGAAAAGTAAAAG	NCBI36
NG_008981.1:g.5617_5618insCTTTTACTTTTCTTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287020.7:c.406+111_406+112insCTTTTACTTTTCTTAAA MANE Select	ENSP00000287020.4:n.406+111_406+112insCTTTTACTTTTCTTAAA
ENST00000287020.6:c.406+111_406+112insCTTTTACTTTTCTTAAA	ENSP00000287020.4:n.406+111_406+112insCTTTTACTTTTCTTAAA
ENST00000620978.1:c.406+111_406+112insCTTTTACTTTTCTTAAA	ENSP00000480170.1:n.406+111_406+112insCTTTTACTTTTCTTAAA
ENST00000621429.1:c.406+111_406+112insCTTTTACTTTTCTTAAA	ENSP00000483711.1:n.406+111_406+112insCTTTTACTTTTCTTAAA
NM_001001557.2:c.406+111_406+112insCTTTTACTTTTCTTAAA	NP_001001557.1:n.406+111_406+112insCTTTTACTTTTCTTAAA
NM_001001557.3:c.406+111_406+112insCTTTTACTTTTCTTAAA	NP_001001557.1:n.406+111_406+112insCTTTTACTTTTCTTAAA
NM_001001557.4:c.406+111_406+112insCTTTTACTTTTCTTAAA MANE Select	NP_001001557.1:n.406+111_406+112insCTTTTACTTTTCTTAAA