Canonical Allele Identifier: CA2639096169

Gene: CA4

Linked Data

• gnomAD v4: 17-60150019-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150019T>A , CM000679.2:g.60150019T>A	GRCh38
NC_000017.10:g.58227380T>A , CM000679.1:g.58227380T>A	GRCh37
NC_000017.9:g.55582162T>A	NCBI36
NG_012050.1:g.5079T>A
NG_012050.2:g.5079T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.-16T>A MANE Select	ENSP00000300900.3:n.-16T>A
ENST00000300900.8:c.-16T>A	ENSP00000300900.3:n.-16T>A
ENST00000585705.5:n.78T>A
ENST00000586876.1:c.-16T>A	ENSP00000467465.1:n.-16T>A
ENST00000591725.1:c.-374T>A	ENSP00000466964.1:n.-374T>A
NM_000717.3:c.-16T>A	NP_000708.1:n.-16T>A
XM_005257639.1:c.-16T>A	XP_005257696.1:n.-16T>A
NM_000717.4:c.-16T>A	NP_000708.1:n.-16T>A
NR_137422.1:n.84T>A
XM_005257639.3:c.-16T>A	XP_005257696.1:n.-16T>A
XR_001752604.2:n.78T>A
XR_001752605.2:n.78T>A
XR_001752606.2:n.78T>A
XR_001752607.2:n.78T>A
XR_001752608.2:n.78T>A
XR_001752609.2:n.78T>A
XR_001752610.2:n.78T>A
NM_000717.5:c.-16T>A MANE Select	NP_000708.1:n.-16T>A
NR_137422.2:n.47T>A