Canonical Allele Identifier: CA2268452091

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150066C= , CM000679.2:g.60150066C=	GRCh38
NC_000017.10:g.58227427C= , CM000679.1:g.58227427C=	GRCh37
NC_000017.9:g.55582209C=	NCBI36
NG_012050.1:g.5126C=
NG_012050.2:g.5126C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.32C= MANE Select	ENSP00000300900.3:p.Ser11=
ENST00000300900.8:c.32C=	ENSP00000300900.3:p.Ser11=
ENST00000585705.5:n.125C=
ENST00000586876.1:c.32C=	ENSP00000467465.1:p.Ser11=
ENST00000591725.1:c.-327C=	ENSP00000466964.1:n.-327C=
NM_000717.3:c.32C=	NP_000708.1:p.Ser11=
XM_005257639.1:c.32C=	XP_005257696.1:p.Ser11=
NM_000717.4:c.32C=	NP_000708.1:p.Ser11=
NR_137422.1:n.131C=
XM_005257639.3:c.32C=	XP_005257696.1:p.Ser11=
XR_001752604.2:n.125C=
XR_001752605.2:n.125C=
XR_001752606.2:n.125C=
XR_001752607.2:n.125C=
XR_001752608.2:n.125C=
XR_001752609.2:n.125C=
XR_001752610.2:n.125C=
NM_000717.5:c.32C= MANE Select	NP_000708.1:p.Ser11=
NR_137422.2:n.94C=