Canonical Allele Identifier: CA2838229675
Gene: ITGA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50076237A>C , CM000679.2:g.50076237A>C GRCh38
NC_000017.10:g.48153601A>C , CM000679.1:g.48153601A>C GRCh37
NC_000017.9:g.45508600A>C NCBI36
NG_029107.2:g.25262A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320031.13:c.1675-89A>C MANE Select ENSP00000315190.8:n.1675-89A>C
ENST00000007722.11:c.1675-89A>C ENSP00000007722.7:n.1675-89A>C
ENST00000320031.12:c.1675-89A>C ENSP00000315190.8:n.1675-89A>C
ENST00000505306.5:n.2047-89A>C
ENST00000505612.1:n.277-89A>C
ENST00000506401.6:c.*1068-89A>C ENSP00000422826.2:n.*1068-89A>C
NM_002204.2:c.1675-89A>C NP_002195.1:n.1675-89A>C
NM_002204.3:c.1675-89A>C NP_002195.1:n.1675-89A>C
NM_005501.2:c.1675-89A>C NP_005492.1:n.1675-89A>C
XM_005257308.1:c.1270-89A>C XP_005257365.1:n.1270-89A>C
XM_005257308.2:c.1270-89A>C XP_005257365.1:n.1270-89A>C
XR_001752507.1:n.2050-89A>C
NM_002204.4:c.1675-89A>C MANE Select NP_002195.1:n.1675-89A>C