Canonical Allele Identifier: CA2268452038

Gene: CA4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60149977G= , CM000679.2:g.60149977G=	GRCh38
NC_000017.10:g.58227338G= , CM000679.1:g.58227338G=	GRCh37
NC_000017.9:g.55582120G=	NCBI36
NG_012050.1:g.5037G=
NG_012050.2:g.5037G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300900.9:c.-58G= MANE Select	ENSP00000300900.3:n.-58G=
ENST00000300900.8:c.-58G=	ENSP00000300900.3:n.-58G=
ENST00000585705.5:n.36G=
ENST00000586876.1:c.-58G=	ENSP00000467465.1:n.-58G=
ENST00000591725.1:c.-416G=	ENSP00000466964.1:n.-416G=
NM_000717.3:c.-58G=	NP_000708.1:n.-58G=
XM_005257639.1:c.-58G=	XP_005257696.1:n.-58G=
NM_000717.4:c.-58G=	NP_000708.1:n.-58G=
NR_137422.1:n.42G=
XM_005257639.3:c.-58G=	XP_005257696.1:n.-58G=
XR_001752604.2:n.36G=
XR_001752605.2:n.36G=
XR_001752606.2:n.36G=
XR_001752607.2:n.36G=
XR_001752608.2:n.36G=
XR_001752609.2:n.36G=
XR_001752610.2:n.36G=
NM_000717.5:c.-58G= MANE Select	NP_000708.1:n.-58G=
NR_137422.2:n.5G=