Canonical Allele Identifier: CA2617530863

Linked Data

gnomAD v4: 12-9079847-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9079847G>T , CM000674.2:g.9079847G>T GRCh38
NC_000012.11:g.9232443G>T , CM000674.1:g.9232443G>T GRCh37
NC_000012.10:g.9123710G>T NCBI36
NG_011717.1:g.41116C>A
NG_011717.2:g.41116C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.2855-32C>A (A2M) MANE Select ENSP00000323929.8:n.2855-32C>A
ENST00000318602.11:c.2855-32C>A (A2M) ENSP00000323929.7:n.2855-32C>A
ENST00000542567.1:n.210-32C>A (A2M)
ENST00000543436.2:n.451+10065C>A (A2M)
ENST00000545828.1:n.349-7126C>A (A2M)
NM_000014.4:c.2855-32C>A (A2M) NP_000005.2:n.2855-32C>A
XM_006719056.2:c.2855-32C>A (A2M) XP_006719119.1:n.2855-32C>A
NM_000014.5:c.2855-32C>A (A2M) NP_000005.2:n.2855-32C>A
NM_001347423.1:c.2855-32C>A (A2M) NP_001334352.1:n.2855-32C>A
NM_001347424.1:c.2555-32C>A (A2M) NP_001334353.1:n.2555-32C>A
NM_001347425.1:c.2405-32C>A (A2M) NP_001334354.1:n.2405-32C>A
XM_006719056.3:c.2855-32C>A (A2M) XP_006719119.1:n.2855-32C>A
XM_017018683.1:c.*33+21681G>T (KLRG1) XP_016874172.1:n.*33+21681G>T
XM_017018684.1:c.*33+21681G>T (KLRG1) XP_016874173.1:n.*33+21681G>T
XM_017018685.1:c.*33+21681G>T (KLRG1) XP_016874174.1:n.*33+21681G>T
NM_000014.6:c.2855-32C>A (A2M) MANE Select NP_000005.3:n.2855-32C>A
NM_001347423.2:c.2855-32C>A (A2M) NP_001334352.2:n.2855-32C>A
NM_001347424.2:c.2555-32C>A (A2M) NP_001334353.2:n.2555-32C>A
NM_001347425.2:c.2405-32C>A (A2M) NP_001334354.2:n.2405-32C>A