Canonical Allele Identifier: CA1152580892
Gene: CA6 HGNC NCBI

Linked Data

dbSNP Id: rs1639714742

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8957306_8957309dup , CM000663.2:g.8957306_8957309dup GRCh38
NC_000001.10:g.9017365_9017368dup , CM000663.1:g.9017365_9017368dup GRCh37
NC_000001.9:g.8939952_8939955dup NCBI36
NG_033975.1:g.16473_16476dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000377443.7:c.408+21_408+24dup MANE Select ENSP00000366662.2:n.408+21_408+24dup
ENST00000377436.6:c.408+21_408+24dup ENSP00000366654.3:n.408+21_408+24dup
ENST00000377442.3:c.228+21_228+24dup ENSP00000366661.2:n.228+21_228+24dup
ENST00000377443.6:c.408+21_408+24dup ENSP00000366662.2:n.408+21_408+24dup
ENST00000476083.1:n.99-1604_99-1601dup
ENST00000549778.5:c.312+21_312+24dup ENSP00000447108.1:n.312+21_312+24dup
NM_001215.3:c.408+21_408+24dup NP_001206.2:n.408+21_408+24dup
NM_001270500.1:c.408+21_408+24dup NP_001257429.1:n.408+21_408+24dup
NM_001270501.1:c.228+21_228+24dup NP_001257430.1:n.228+21_228+24dup
NM_001270502.1:c.25-1604_25-1601dup NP_001257431.1:n.25-1604_25-1601dup
XM_011542083.1:c.420+21_420+24dup XP_011540385.1:n.420+21_420+24dup
XM_011542084.1:c.420+21_420+24dup XP_011540386.1:n.420+21_420+24dup
XM_011542083.3:c.420+21_420+24dup XP_011540385.1:n.420+21_420+24dup
XM_011542084.3:c.420+21_420+24dup XP_011540386.1:n.420+21_420+24dup
NM_001215.4:c.408+21_408+24dup MANE Select NP_001206.2:n.408+21_408+24dup
NM_001270500.2:c.408+21_408+24dup NP_001257429.1:n.408+21_408+24dup
NM_001270501.2:c.228+21_228+24dup NP_001257430.1:n.228+21_228+24dup
NM_001270502.2:c.25-1604_25-1601dup NP_001257431.1:n.25-1604_25-1601dup