Canonical Allele Identifier: CA2617530876

Linked Data

gnomAD v4: 12-9079859-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9079859T>A , CM000674.2:g.9079859T>A GRCh38
NC_000012.11:g.9232455T>A , CM000674.1:g.9232455T>A GRCh37
NC_000012.10:g.9123722T>A NCBI36
NG_011717.1:g.41104A>T
NG_011717.2:g.41104A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.2855-44A>T (A2M) MANE Select ENSP00000323929.8:n.2855-44A>T
ENST00000318602.11:c.2855-44A>T (A2M) ENSP00000323929.7:n.2855-44A>T
ENST00000542567.1:n.210-44A>T (A2M)
ENST00000543436.2:n.451+10053A>T (A2M)
ENST00000545828.1:n.349-7138A>T (A2M)
NM_000014.4:c.2855-44A>T (A2M) NP_000005.2:n.2855-44A>T
XM_006719056.2:c.2855-44A>T (A2M) XP_006719119.1:n.2855-44A>T
NM_000014.5:c.2855-44A>T (A2M) NP_000005.2:n.2855-44A>T
NM_001347423.1:c.2855-44A>T (A2M) NP_001334352.1:n.2855-44A>T
NM_001347424.1:c.2555-44A>T (A2M) NP_001334353.1:n.2555-44A>T
NM_001347425.1:c.2405-44A>T (A2M) NP_001334354.1:n.2405-44A>T
XM_006719056.3:c.2855-44A>T (A2M) XP_006719119.1:n.2855-44A>T
XM_017018683.1:c.*33+21693T>A (KLRG1) XP_016874172.1:n.*33+21693T>A
XM_017018684.1:c.*33+21693T>A (KLRG1) XP_016874173.1:n.*33+21693T>A
XM_017018685.1:c.*33+21693T>A (KLRG1) XP_016874174.1:n.*33+21693T>A
NM_000014.6:c.2855-44A>T (A2M) MANE Select NP_000005.3:n.2855-44A>T
NM_001347423.2:c.2855-44A>T (A2M) NP_001334352.2:n.2855-44A>T
NM_001347424.2:c.2555-44A>T (A2M) NP_001334353.2:n.2555-44A>T
NM_001347425.2:c.2405-44A>T (A2M) NP_001334354.2:n.2405-44A>T