Canonical Allele Identifier: CA2639096116

Gene: CA4

Linked Data

• gnomAD v4: 17-60149982-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60149982G>A , CM000679.2:g.60149982G>A	GRCh38
NC_000017.10:g.58227343G>A , CM000679.1:g.58227343G>A	GRCh37
NC_000017.9:g.55582125G>A	NCBI36
NG_012050.1:g.5042G>A
NG_012050.2:g.5042G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300900.9:c.-53G>A MANE Select	ENSP00000300900.3:n.-53G>A
ENST00000300900.8:c.-53G>A	ENSP00000300900.3:n.-53G>A
ENST00000585705.5:n.41G>A
ENST00000586876.1:c.-53G>A	ENSP00000467465.1:n.-53G>A
ENST00000591725.1:c.-411G>A	ENSP00000466964.1:n.-411G>A
NM_000717.3:c.-53G>A	NP_000708.1:n.-53G>A
XM_005257639.1:c.-53G>A	XP_005257696.1:n.-53G>A
NM_000717.4:c.-53G>A	NP_000708.1:n.-53G>A
NR_137422.1:n.47G>A
XM_005257639.3:c.-53G>A	XP_005257696.1:n.-53G>A
XR_001752604.2:n.41G>A
XR_001752605.2:n.41G>A
XR_001752606.2:n.41G>A
XR_001752607.2:n.41G>A
XR_001752608.2:n.41G>A
XR_001752609.2:n.41G>A
XR_001752610.2:n.41G>A
NM_000717.5:c.-53G>A MANE Select	NP_000708.1:n.-53G>A
NR_137422.2:n.10G>A