Canonical Allele Identifier: CA2838711457

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150033dup , CM000679.2:g.60150033dup	GRCh38
NC_000017.10:g.58227394dup , CM000679.1:g.58227394dup	GRCh37
NC_000017.9:g.55582176dup	NCBI36
NG_012050.1:g.5093dup
NG_012050.2:g.5093dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.-2dup MANE Select	ENSP00000300900.3:n.-2dup
ENST00000300900.8:c.-2dup	ENSP00000300900.3:n.-2dup
ENST00000585705.5:n.92dup
ENST00000586876.1:c.-2dup	ENSP00000467465.1:n.-2dup
ENST00000591725.1:c.-360dup	ENSP00000466964.1:n.-360dup
NM_000717.3:c.-2dup	NP_000708.1:n.-2dup
XM_005257639.1:c.-2dup	XP_005257696.1:n.-2dup
NM_000717.4:c.-2dup	NP_000708.1:n.-2dup
NR_137422.1:n.98dup
XM_005257639.3:c.-2dup	XP_005257696.1:n.-2dup
XR_001752604.2:n.92dup
XR_001752605.2:n.92dup
XR_001752606.2:n.92dup
XR_001752607.2:n.92dup
XR_001752608.2:n.92dup
XR_001752609.2:n.92dup
XR_001752610.2:n.92dup
NM_000717.5:c.-2dup MANE Select	NP_000708.1:n.-2dup
NR_137422.2:n.61dup