Canonical Allele Identifier: CA2678127466

Gene: AGER

Linked Data

• gnomAD v4: 6-32181776-GGTGCGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32181777_32181782del , CM000668.2:g.32181777_32181782del	GRCh38
NC_000006.11:g.32149554_32149559del , CM000668.1:g.32149554_32149559del	GRCh37
NC_000006.10:g.32257532_32257537del	NCBI36
NG_029868.1:g.7541_7546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375076.9:c.965-150_965-145del MANE Select	ENSP00000364217.4:n.965-150_965-145del
ENST00000375055.6:c.965-150_965-145del	ENSP00000364195.2:n.965-150_965-145del
ENST00000375065.6:c.152-150_152-145del	ENSP00000364206.6:n.152-150_152-145del
ENST00000375067.7:c.810-150_810-145del	ENSP00000364208.3:n.810-150_810-145del
ENST00000375069.7:c.1013-150_1013-145del	ENSP00000364210.4:n.1013-150_1013-145del
ENST00000375070.7:c.662-305_662-300del	ENSP00000364211.4:n.662-305_662-300del
ENST00000375076.8:c.965-150_965-145del	ENSP00000364217.4:n.965-150_965-145del
ENST00000438221.6:c.1013-150_1013-145del	ENSP00000387887.2:n.1013-150_1013-145del
ENST00000473619.5:n.507-150_507-145del
ENST00000484849.5:n.1172-150_1172-145del
ENST00000488669.5:n.507-150_507-145del
ENST00000620802.4:c.283-349_283-344del	ENSP00000484081.1:n.283-349_283-344del
NM_001136.4:c.965-150_965-145del	NP_001127.1:n.965-150_965-145del
NM_001206929.1:c.1013-150_1013-145del	NP_001193858.1:n.1013-150_1013-145del
NM_001206932.1:c.923-150_923-145del	NP_001193861.1:n.923-150_923-145del
NM_001206934.1:c.1013-150_1013-145del	NP_001193863.1:n.1013-150_1013-145del
NM_001206936.1:c.913-150_913-145del	NP_001193865.1:n.913-150_913-145del
NM_001206940.1:c.965-150_965-145del	NP_001193869.1:n.965-150_965-145del
NM_001206954.1:c.823-150_823-145del	NP_001193883.1:n.823-150_823-145del
NM_001206966.1:c.965-150_965-145del	NP_001193895.1:n.965-150_965-145del
NM_172197.2:c.810-150_810-145del	NP_751947.1:n.810-150_810-145del
NR_038190.1:n.1248-150_1248-145del
XM_017010328.2:c.964-150_964-145del	XP_016865817.1:n.964-150_964-145del
XR_001743189.2:n.1029-150_1029-145del
XR_001743190.2:n.981-150_981-145del
NM_001136.5:c.965-150_965-145del MANE Select	NP_001127.1:n.965-150_965-145del
NM_001206932.2:c.923-150_923-145del	NP_001193861.1:n.923-150_923-145del
NM_001206936.2:c.913-150_913-145del	NP_001193865.1:n.913-150_913-145del
NM_001206940.2:c.965-150_965-145del	NP_001193869.1:n.965-150_965-145del
NM_001206954.2:c.823-150_823-145del	NP_001193883.1:n.823-150_823-145del
NM_001206966.2:c.965-150_965-145del	NP_001193895.1:n.965-150_965-145del
NM_172197.3:c.810-150_810-145del	NP_751947.1:n.810-150_810-145del
NR_038190.2:n.1179-150_1179-145del
NM_001206929.2:c.1013-150_1013-145del	NP_001193858.1:n.1013-150_1013-145del
NM_001206934.2:c.1013-150_1013-145del	NP_001193863.1:n.1013-150_1013-145del