Canonical Allele Identifier: CA620489703
Gene: CORO7 HGNC NCBI
CORO7-PAM16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4388642C>G , CM000678.2:g.4388642C>G GRCh38
NC_000016.9:g.4438643C>G , CM000678.1:g.4438643C>G GRCh37
NC_000016.8:g.4378644C>G NCBI36
NG_052966.1:g.33320G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251166.9:c.616-11G>C (CORO7) MANE Select ENSP00000251166.4:n.616-11G>C
ENST00000251166.8:c.616-11G>C (CORO7) ENSP00000251166.4:n.616-11G>C
ENST00000537233.6:c.562-11G>C (CORO7) ENSP00000440460.2:n.562-11G>C
ENST00000570645.5:c.117-11G>C (CORO7) ENSP00000460901.1:n.117-11G>C
ENST00000571052.5:c.117-11G>C (CORO7) ENSP00000459085.1:n.117-11G>C
ENST00000571059.5:c.337-20G>C (CORO7) ENSP00000460036.1:n.337-20G>C
ENST00000571227.5:c.*552-11G>C (CORO7) ENSP00000458459.1:n.*552-11G>C
ENST00000571756.5:c.555-11G>C (CORO7) ENSP00000458828.1:n.555-11G>C
ENST00000572044.1:c.112-11G>C (CORO7) ENSP00000458411.1:n.112-11G>C
ENST00000572467.5:c.616-11G>C (CORO7-PAM16) ENSP00000460885.1:n.616-11G>C
ENST00000572549.5:c.151-11G>C (CORO7) ENSP00000459286.1:n.151-11G>C
ENST00000573245.1:n.53-11G>C (CORO7)
ENST00000574025.5:c.361-11G>C (CORO7) ENSP00000461702.1:n.361-11G>C
ENST00000574311.5:c.112-11G>C (CORO7) ENSP00000461187.1:n.112-11G>C
ENST00000575038.5:c.555-11G>C (CORO7) ENSP00000461797.1:n.555-11G>C
ENST00000575334.5:c.616-11G>C (CORO7-PAM16) ENSP00000458607.1:n.616-11G>C
ENST00000575714.5:n.145-11G>C (CORO7)
ENST00000576437.5:c.116+6647G>C (CORO7) ENSP00000459228.1:n.116+6647G>C
NM_001201472.1:c.562-11G>C (CORO7) NP_001188401.1:n.562-11G>C
NM_001201473.1:c.361-11G>C (CORO7) NP_001188402.1:n.361-11G>C
NM_001201479.1:c.616-11G>C (CORO7-PAM16) NP_001188408.1:n.616-11G>C
NM_024535.4:c.616-11G>C (CORO7) NP_078811.3:n.616-11G>C
NM_001351729.1:c.-45-11G>C (CORO7) NP_001338658.1:n.-45-11G>C
NM_024535.5:c.616-11G>C (CORO7) MANE Select NP_078811.3:n.616-11G>C
NM_001201472.2:c.562-11G>C (CORO7) NP_001188401.1:n.562-11G>C
NM_001201473.2:c.361-11G>C (CORO7) NP_001188402.1:n.361-11G>C
NM_001201479.2:c.616-11G>C (CORO7-PAM16) NP_001188408.1:n.616-11G>C
NM_001351729.2:c.-45-11G>C (CORO7) NP_001338658.1:n.-45-11G>C