Canonical Allele Identifier: CA2639096154

Gene: CA4

Linked Data

• gnomAD v4: 17-60150008-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150008T>G , CM000679.2:g.60150008T>G	GRCh38
NC_000017.10:g.58227369T>G , CM000679.1:g.58227369T>G	GRCh37
NC_000017.9:g.55582151T>G	NCBI36
NG_012050.1:g.5068T>G
NG_012050.2:g.5068T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.-27T>G MANE Select	ENSP00000300900.3:n.-27T>G
ENST00000300900.8:c.-27T>G	ENSP00000300900.3:n.-27T>G
ENST00000585705.5:n.67T>G
ENST00000586876.1:c.-27T>G	ENSP00000467465.1:n.-27T>G
ENST00000591725.1:c.-385T>G	ENSP00000466964.1:n.-385T>G
NM_000717.3:c.-27T>G	NP_000708.1:n.-27T>G
XM_005257639.1:c.-27T>G	XP_005257696.1:n.-27T>G
NM_000717.4:c.-27T>G	NP_000708.1:n.-27T>G
NR_137422.1:n.73T>G
XM_005257639.3:c.-27T>G	XP_005257696.1:n.-27T>G
XR_001752604.2:n.67T>G
XR_001752605.2:n.67T>G
XR_001752606.2:n.67T>G
XR_001752607.2:n.67T>G
XR_001752608.2:n.67T>G
XR_001752609.2:n.67T>G
XR_001752610.2:n.67T>G
NM_000717.5:c.-27T>G MANE Select	NP_000708.1:n.-27T>G
NR_137422.2:n.36T>G