Canonical Allele Identifier: CA2643090530

Gene: CA6

Linked Data

• gnomAD v4: 1-8957018-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957020del , CM000663.2:g.8957020del	GRCh38
NC_000001.10:g.9017079del , CM000663.1:g.9017079del	GRCh37
NC_000001.9:g.8939666del	NCBI36
NG_033975.1:g.16187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.260-117del MANE Select	ENSP00000366662.2:n.260-117del
ENST00000377436.6:c.260-117del	ENSP00000366654.3:n.260-117del
ENST00000377442.3:c.80-117del	ENSP00000366661.2:n.80-117del
ENST00000377443.6:c.260-117del	ENSP00000366662.2:n.260-117del
ENST00000476083.1:n.99-1890del
ENST00000549778.5:c.169-122del	ENSP00000447108.1:n.169-122del
NM_001215.3:c.260-117del	NP_001206.2:n.260-117del
NM_001270500.1:c.260-117del	NP_001257429.1:n.260-117del
NM_001270501.1:c.80-117del	NP_001257430.1:n.80-117del
NM_001270502.1:c.25-1890del	NP_001257431.1:n.25-1890del
XM_011542083.1:c.272-117del	XP_011540385.1:n.272-117del
XM_011542084.1:c.272-117del	XP_011540386.1:n.272-117del
XM_011542083.3:c.272-117del	XP_011540385.1:n.272-117del
XM_011542084.3:c.272-117del	XP_011540386.1:n.272-117del
NM_001215.4:c.260-117del MANE Select	NP_001206.2:n.260-117del
NM_001270500.2:c.260-117del	NP_001257429.1:n.260-117del
NM_001270501.2:c.80-117del	NP_001257430.1:n.80-117del
NM_001270502.2:c.25-1890del	NP_001257431.1:n.25-1890del