Canonical Allele Identifier: CA6438332

Linked Data

dbSNP Id: rs1555156916

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9090026_9090027insT , CM000674.2:g.9090026_9090027insT GRCh38
NC_000012.11:g.9242622_9242623insT , CM000674.1:g.9242622_9242623insT GRCh37
NC_000012.10:g.9133889_9133890insT NCBI36
NG_011717.1:g.30936_30937insA
NG_011717.2:g.30936_30937insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.2597-4_2597-3insA (A2M) MANE Select ENSP00000323929.8:n.2597-4_2597-3insA
ENST00000318602.11:c.2597-4_2597-3insA (A2M) ENSP00000323929.7:n.2597-4_2597-3insA
ENST00000462568.1:n.176-4_176-3insA (A2M)
ENST00000543436.2:n.340-4_340-3insA (A2M)
ENST00000545828.1:n.348+11523_348+11524insA (A2M)
NM_000014.4:c.2597-4_2597-3insA (A2M) NP_000005.2:n.2597-4_2597-3insA
XM_006719056.2:c.2597-4_2597-3insA (A2M) XP_006719119.1:n.2597-4_2597-3insA
NM_000014.5:c.2597-4_2597-3insA (A2M) NP_000005.2:n.2597-4_2597-3insA
NM_001347423.1:c.2597-4_2597-3insA (A2M) NP_001334352.1:n.2597-4_2597-3insA
NM_001347424.1:c.2297-4_2297-3insA (A2M) NP_001334353.1:n.2297-4_2297-3insA
NM_001347425.1:c.2147-4_2147-3insA (A2M) NP_001334354.1:n.2147-4_2147-3insA
XM_006719056.3:c.2597-4_2597-3insA (A2M) XP_006719119.1:n.2597-4_2597-3insA
XM_017018683.1:c.*33+31860_*33+31861insT (KLRG1) XP_016874172.1:n.*33+31860_*33+31861insT
XM_017018684.1:c.*33+31860_*33+31861insT (KLRG1) XP_016874173.1:n.*33+31860_*33+31861insT
XM_017018685.1:c.*33+31860_*33+31861insT (KLRG1) XP_016874174.1:n.*33+31860_*33+31861insT
NM_000014.6:c.2597-4_2597-3insA (A2M) MANE Select NP_000005.3:n.2597-4_2597-3insA
NM_001347423.2:c.2597-4_2597-3insA (A2M) NP_001334352.2:n.2597-4_2597-3insA
NM_001347424.2:c.2297-4_2297-3insA (A2M) NP_001334353.2:n.2297-4_2297-3insA
NM_001347425.2:c.2147-4_2147-3insA (A2M) NP_001334354.2:n.2147-4_2147-3insA