Canonical Allele Identifier: CA2271191712

Gene: APOH

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66227875_66227886delinsCCAAGACCTTCT , CM000679.2:g.66227875_66227886delinsCCAAGACCTTCT	GRCh38
NC_000017.10:g.64223993_64224004delinsCCAAGACCTTCT , CM000679.1:g.64223993_64224004delinsCCAAGACCTTCT	GRCh37
NC_000017.9:g.61654455_61654466delinsCCAAGACCTTCT	NCBI36
NG_012045.1:g.6553_6564delinsAGAAGGTCTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.241+134_241+145delinsAGAAGGTCTTGG MANE Select	ENSP00000205948.6:n.241+134_241+145delinsAGAAGGTCTTGG
ENST00000205948.10:c.241+134_241+145delinsAGAAGGTCTTGG	ENSP00000205948.6:n.241+134_241+145delinsAGAAGGTCTTGG
ENST00000577982.1:c.241+134_241+145delinsAGAAGGTCTTGG	ENSP00000464301.1:n.241+134_241+145delinsAGAAGGTCTTGG
ENST00000581797.5:c.61+134_61+145delinsAGAAGGTCTTGG	ENSP00000463553.1:n.61+134_61+145delinsAGAAGGTCTTGG
NM_000042.2:c.241+134_241+145delinsAGAAGGTCTTGG	NP_000033.2:n.241+134_241+145delinsAGAAGGTCTTGG
NM_000042.3:c.241+134_241+145delinsAGAAGGTCTTGG MANE Select	NP_000033.2:n.241+134_241+145delinsAGAAGGTCTTGG