Canonical Allele Identifier: CA1937420446

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570955_113570957delinsATC , CM000672.2:g.113570955_113570957delinsATC	GRCh38
NC_000010.10:g.115330714_115330716delinsATC , CM000672.1:g.115330714_115330716delinsATC	GRCh37
NC_000010.9:g.115320704_115320706delinsATC	NCBI36
NG_008956.1:g.22937_22939delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-3334_107-3332delinsATC MANE Select	ENSP00000277903.4:n.107-3334_107-3332delinsATC
ENST00000351270.3:c.107-3334_107-3332delinsATC	ENSP00000277903.4:n.107-3334_107-3332delinsATC
ENST00000542051.5:c.29-3334_29-3332delinsATC	ENSP00000443283.1:n.29-3334_29-3332delinsATC
NM_001177660.1:c.29-3334_29-3332delinsATC	NP_001171131.1:n.29-3334_29-3332delinsATC
NM_004132.3:c.107-3334_107-3332delinsATC	NP_004123.1:n.107-3334_107-3332delinsATC
NM_001177660.2:c.29-3334_29-3332delinsATC	NP_001171131.1:n.29-3334_29-3332delinsATC
NM_004132.4:c.107-3334_107-3332delinsATC	NP_004123.1:n.107-3334_107-3332delinsATC
NM_004132.5:c.107-3334_107-3332delinsATC MANE Select	NP_004123.1:n.107-3334_107-3332delinsATC
NM_001177660.3:c.29-3334_29-3332delinsATC	NP_001171131.1:n.29-3334_29-3332delinsATC