Canonical Allele Identifier: CA1937420327

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570731_113570732delinsAT , CM000672.2:g.113570731_113570732delinsAT	GRCh38
NC_000010.10:g.115330490_115330491delinsAT , CM000672.1:g.115330490_115330491delinsAT	GRCh37
NC_000010.9:g.115320480_115320481delinsAT	NCBI36
NG_008956.1:g.22713_22714delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.106+3206_106+3207delinsAT MANE Select	ENSP00000277903.4:n.106+3206_106+3207delinsAT
ENST00000351270.3:c.106+3206_106+3207delinsAT	ENSP00000277903.4:n.106+3206_106+3207delinsAT
ENST00000542051.5:c.28+3206_28+3207delinsAT	ENSP00000443283.1:n.28+3206_28+3207delinsAT
NM_001177660.1:c.28+3206_28+3207delinsAT	NP_001171131.1:n.28+3206_28+3207delinsAT
NM_004132.3:c.106+3206_106+3207delinsAT	NP_004123.1:n.106+3206_106+3207delinsAT
NM_001177660.2:c.28+3206_28+3207delinsAT	NP_001171131.1:n.28+3206_28+3207delinsAT
NM_004132.4:c.106+3206_106+3207delinsAT	NP_004123.1:n.106+3206_106+3207delinsAT
NM_004132.5:c.106+3206_106+3207delinsAT MANE Select	NP_004123.1:n.106+3206_106+3207delinsAT
NM_001177660.3:c.28+3206_28+3207delinsAT	NP_001171131.1:n.28+3206_28+3207delinsAT