Canonical Allele Identifier: CA1152580940

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957340_8957344delinsCTTTT , CM000663.2:g.8957340_8957344delinsCTTTT	GRCh38
NC_000001.10:g.9017399_9017403delinsCTTTT , CM000663.1:g.9017399_9017403delinsCTTTT	GRCh37
NC_000001.9:g.8939986_8939990delinsCTTTT	NCBI36
NG_033975.1:g.16507_16511delinsCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.408+55_408+59delinsCTTTT MANE Select	ENSP00000366662.2:n.408+55_408+59delinsCTTTT
ENST00000377436.6:c.408+55_408+59delinsCTTTT	ENSP00000366654.3:n.408+55_408+59delinsCTTTT
ENST00000377442.3:c.228+55_228+59delinsCTTTT	ENSP00000366661.2:n.228+55_228+59delinsCTTTT
ENST00000377443.6:c.408+55_408+59delinsCTTTT	ENSP00000366662.2:n.408+55_408+59delinsCTTTT
ENST00000476083.1:n.99-1570_99-1566delinsCTTTT
ENST00000549778.5:c.312+55_312+59delinsCTTTT	ENSP00000447108.1:n.312+55_312+59delinsCTTTT
NM_001215.3:c.408+55_408+59delinsCTTTT	NP_001206.2:n.408+55_408+59delinsCTTTT
NM_001270500.1:c.408+55_408+59delinsCTTTT	NP_001257429.1:n.408+55_408+59delinsCTTTT
NM_001270501.1:c.228+55_228+59delinsCTTTT	NP_001257430.1:n.228+55_228+59delinsCTTTT
NM_001270502.1:c.25-1570_25-1566delinsCTTTT	NP_001257431.1:n.25-1570_25-1566delinsCTTTT
XM_011542083.1:c.420+55_420+59delinsCTTTT	XP_011540385.1:n.420+55_420+59delinsCTTTT
XM_011542084.1:c.420+55_420+59delinsCTTTT	XP_011540386.1:n.420+55_420+59delinsCTTTT
XM_011542083.3:c.420+55_420+59delinsCTTTT	XP_011540385.1:n.420+55_420+59delinsCTTTT
XM_011542084.3:c.420+55_420+59delinsCTTTT	XP_011540386.1:n.420+55_420+59delinsCTTTT
NM_001215.4:c.408+55_408+59delinsCTTTT MANE Select	NP_001206.2:n.408+55_408+59delinsCTTTT
NM_001270500.2:c.408+55_408+59delinsCTTTT	NP_001257429.1:n.408+55_408+59delinsCTTTT
NM_001270501.2:c.228+55_228+59delinsCTTTT	NP_001257430.1:n.228+55_228+59delinsCTTTT
NM_001270502.2:c.25-1570_25-1566delinsCTTTT	NP_001257431.1:n.25-1570_25-1566delinsCTTTT