Canonical Allele Identifier: CA660059996

Gene: HABP2

Linked Data

• dbSNP Id: rs1404670645
• MyVariant Identifiers: chr10:g.115331032_115331033insTGTCT (hg19) ; chr10:g.113571273_113571274insTGTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113571274_113571275insGTCTT , CM000672.2:g.113571274_113571275insGTCTT	GRCh38
NC_000010.10:g.115331033_115331034insGTCTT , CM000672.1:g.115331033_115331034insGTCTT	GRCh37
NC_000010.9:g.115321023_115321024insGTCTT	NCBI36
NG_008956.1:g.23256_23257insGTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-3015_107-3014insGTCTT MANE Select	ENSP00000277903.4:n.107-3015_107-3014insGTCTT
ENST00000351270.3:c.107-3015_107-3014insGTCTT	ENSP00000277903.4:n.107-3015_107-3014insGTCTT
ENST00000542051.5:c.29-3015_29-3014insGTCTT	ENSP00000443283.1:n.29-3015_29-3014insGTCTT
NM_001177660.1:c.29-3015_29-3014insGTCTT	NP_001171131.1:n.29-3015_29-3014insGTCTT
NM_004132.3:c.107-3015_107-3014insGTCTT	NP_004123.1:n.107-3015_107-3014insGTCTT
NM_001177660.2:c.29-3015_29-3014insGTCTT	NP_001171131.1:n.29-3015_29-3014insGTCTT
NM_004132.4:c.107-3015_107-3014insGTCTT	NP_004123.1:n.107-3015_107-3014insGTCTT
NM_004132.5:c.107-3015_107-3014insGTCTT MANE Select	NP_004123.1:n.107-3015_107-3014insGTCTT
NM_001177660.3:c.29-3015_29-3014insGTCTT	NP_001171131.1:n.29-3015_29-3014insGTCTT