Canonical Allele Identifier: CA2617528451

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9068945_9068946insCCTC , CM000674.2:g.9068945_9068946insCCTC GRCh38
NC_000012.11:g.9221541_9221542insCCTC , CM000674.1:g.9221541_9221542insCCTC GRCh37
NC_000012.10:g.9112808_9112809insCCTC NCBI36
NG_011717.1:g.52018_52019insAGGG
NG_011717.2:g.52018_52019insAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.12:c.4264-103_4264-102insAGGG (A2M) MANE Select ENSP00000323929.8:n.4264-103_4264-102insAGGG
ENST00000318602.11:c.4264-103_4264-102insAGGG (A2M) ENSP00000323929.7:n.4264-103_4264-102insAGGG
ENST00000495442.1:n.11_12insAGGG (A2M)
ENST00000495709.1:n.134_135insAGGG (A2M)
ENST00000543436.2:n.452-1133_452-1132insAGGG (A2M)
NM_000014.4:c.4264-103_4264-102insAGGG (A2M) NP_000005.2:n.4264-103_4264-102insAGGG
XM_006719056.2:c.4264-103_4264-102insAGGG (A2M) XP_006719119.1:n.4264-103_4264-102insAGGG
NM_000014.5:c.4264-103_4264-102insAGGG (A2M) NP_000005.2:n.4264-103_4264-102insAGGG
NM_001347423.1:c.4264-103_4264-102insAGGG (A2M) NP_001334352.1:n.4264-103_4264-102insAGGG
NM_001347424.1:c.3964-103_3964-102insAGGG (A2M) NP_001334353.1:n.3964-103_3964-102insAGGG
NM_001347425.1:c.3814-103_3814-102insAGGG (A2M) NP_001334354.1:n.3814-103_3814-102insAGGG
XM_006719056.3:c.4264-103_4264-102insAGGG (A2M) XP_006719119.1:n.4264-103_4264-102insAGGG
XM_017018683.1:c.*33+10779_*33+10780insCCTC (KLRG1) XP_016874172.1:n.*33+10779_*33+10780insCCTC
XM_017018684.1:c.*33+10779_*33+10780insCCTC (KLRG1) XP_016874173.1:n.*33+10779_*33+10780insCCTC
XM_017018685.1:c.*33+10779_*33+10780insCCTC (KLRG1) XP_016874174.1:n.*33+10779_*33+10780insCCTC
NM_000014.6:c.4264-103_4264-102insAGGG (A2M) MANE Select NP_000005.3:n.4264-103_4264-102insAGGG
NM_001347423.2:c.4264-103_4264-102insAGGG (A2M) NP_001334352.2:n.4264-103_4264-102insAGGG
NM_001347424.2:c.3964-103_3964-102insAGGG (A2M) NP_001334353.2:n.3964-103_3964-102insAGGG
NM_001347425.2:c.3814-103_3814-102insAGGG (A2M) NP_001334354.2:n.3814-103_3814-102insAGGG