Canonical Allele Identifier: CA656824645

Gene: CA4

Linked Data

• COSMIC: COSN15662696

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60149976_60149977insT , CM000679.2:g.60149976_60149977insT	GRCh38
NC_000017.10:g.58227337_58227338insT , CM000679.1:g.58227337_58227338insT	GRCh37
NC_000017.9:g.55582119_55582120insT	NCBI36
NG_012050.1:g.5036_5037insT
NG_012050.2:g.5036_5037insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000300900.9:c.-59_-58insT MANE Select	ENSP00000300900.3:n.-59_-58insT
ENST00000300900.8:c.-59_-58insT	ENSP00000300900.3:n.-59_-58insT
ENST00000585705.5:n.35_36insT
ENST00000586876.1:c.-59_-58insT	ENSP00000467465.1:n.-59_-58insT
ENST00000591725.1:c.-417_-416insT	ENSP00000466964.1:n.-417_-416insT
NM_000717.3:c.-59_-58insT	NP_000708.1:n.-59_-58insT
XM_005257639.1:c.-59_-58insT	XP_005257696.1:n.-59_-58insT
NM_000717.4:c.-59_-58insT	NP_000708.1:n.-59_-58insT
NR_137422.1:n.41_42insT
XM_005257639.3:c.-59_-58insT	XP_005257696.1:n.-59_-58insT
XR_001752604.2:n.35_36insT
XR_001752605.2:n.35_36insT
XR_001752606.2:n.35_36insT
XR_001752607.2:n.35_36insT
XR_001752608.2:n.35_36insT
XR_001752609.2:n.35_36insT
XR_001752610.2:n.35_36insT
NM_000717.5:c.-59_-58insT MANE Select	NP_000708.1:n.-59_-58insT
NR_137422.2:n.4_5insT