Canonical Allele Identifier: CA501125162

Gene: CA4

Linked Data

• MyVariant Identifiers: chr17:g.58227452A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.60150091A>T , CM000679.2:g.60150091A>T	GRCh38
NC_000017.10:g.58227452A>T , CM000679.1:g.58227452A>T	GRCh37
NC_000017.9:g.55582234A>T	NCBI36
NG_012050.1:g.5151A>T
NG_012050.2:g.5151A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300900.9:c.57A>T MANE Select	ENSP00000300900.3:p.Ala19=
ENST00000300900.8:c.57A>T	ENSP00000300900.3:p.Ala19=
ENST00000585705.5:n.150A>T
ENST00000586876.1:c.57A>T	ENSP00000467465.1:p.Ala19=
ENST00000591725.1:c.-302A>T	ENSP00000466964.1:n.-302A>T
NM_000717.3:c.57A>T	NP_000708.1:p.Ala19=
XM_005257639.1:c.57A>T	XP_005257696.1:p.Ala19=
NM_000717.4:c.57A>T	NP_000708.1:p.Ala19=
NR_137422.1:n.156A>T
XM_005257639.3:c.57A>T	XP_005257696.1:p.Ala19=
XR_001752604.2:n.150A>T
XR_001752605.2:n.150A>T
XR_001752606.2:n.150A>T
XR_001752607.2:n.150A>T
XR_001752608.2:n.150A>T
XR_001752609.2:n.150A>T
XR_001752610.2:n.150A>T
NM_000717.5:c.57A>T MANE Select	NP_000708.1:p.Ala19=
NR_137422.2:n.119A>T