Canonical Allele Identifier: CA2643090589
Gene: CA6 HGNC NCBI

Linked Data

gnomAD v4: 1-8957061-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8957061G>A , CM000663.2:g.8957061G>A GRCh38
NC_000001.10:g.9017120G>A , CM000663.1:g.9017120G>A GRCh37
NC_000001.9:g.8939707G>A NCBI36
NG_033975.1:g.16228G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377443.7:c.260-76G>A MANE Select ENSP00000366662.2:n.260-76G>A
ENST00000377436.6:c.260-76G>A ENSP00000366654.3:n.260-76G>A
ENST00000377442.3:c.80-76G>A ENSP00000366661.2:n.80-76G>A
ENST00000377443.6:c.260-76G>A ENSP00000366662.2:n.260-76G>A
ENST00000476083.1:n.99-1849G>A
ENST00000549778.5:c.169-81G>A ENSP00000447108.1:n.169-81G>A
NM_001215.3:c.260-76G>A NP_001206.2:n.260-76G>A
NM_001270500.1:c.260-76G>A NP_001257429.1:n.260-76G>A
NM_001270501.1:c.80-76G>A NP_001257430.1:n.80-76G>A
NM_001270502.1:c.25-1849G>A NP_001257431.1:n.25-1849G>A
XM_011542083.1:c.272-76G>A XP_011540385.1:n.272-76G>A
XM_011542084.1:c.272-76G>A XP_011540386.1:n.272-76G>A
XM_011542083.3:c.272-76G>A XP_011540385.1:n.272-76G>A
XM_011542084.3:c.272-76G>A XP_011540386.1:n.272-76G>A
NM_001215.4:c.260-76G>A MANE Select NP_001206.2:n.260-76G>A
NM_001270500.2:c.260-76G>A NP_001257429.1:n.260-76G>A
NM_001270501.2:c.80-76G>A NP_001257430.1:n.80-76G>A
NM_001270502.2:c.25-1849G>A NP_001257431.1:n.25-1849G>A