Canonical Allele Identifier: CA501125131

Gene: CA4

Linked Data

• MyVariant Identifiers: chr17:g.58227431G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150070G>C , CM000679.2:g.60150070G>C	GRCh38
NC_000017.10:g.58227431G>C , CM000679.1:g.58227431G>C	GRCh37
NC_000017.9:g.55582213G>C	NCBI36
NG_012050.1:g.5130G>C
NG_012050.2:g.5130G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.36G>C MANE Select	ENSP00000300900.3:p.Ala12=
ENST00000300900.8:c.36G>C	ENSP00000300900.3:p.Ala12=
ENST00000585705.5:n.129G>C
ENST00000586876.1:c.36G>C	ENSP00000467465.1:p.Ala12=
ENST00000591725.1:c.-323G>C	ENSP00000466964.1:n.-323G>C
NM_000717.3:c.36G>C	NP_000708.1:p.Ala12=
XM_005257639.1:c.36G>C	XP_005257696.1:p.Ala12=
NM_000717.4:c.36G>C	NP_000708.1:p.Ala12=
NR_137422.1:n.135G>C
XM_005257639.3:c.36G>C	XP_005257696.1:p.Ala12=
XR_001752604.2:n.129G>C
XR_001752605.2:n.129G>C
XR_001752606.2:n.129G>C
XR_001752607.2:n.129G>C
XR_001752608.2:n.129G>C
XR_001752609.2:n.129G>C
XR_001752610.2:n.129G>C
NM_000717.5:c.36G>C MANE Select	NP_000708.1:p.Ala12=
NR_137422.2:n.98G>C