Canonical Allele Identifier: CA1937429087

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588144_113588145delinsTG , CM000672.2:g.113588144_113588145delinsTG	GRCh38
NC_000010.10:g.115347903_115347904delinsTG , CM000672.1:g.115347903_115347904delinsTG	GRCh37
NC_000010.9:g.115337893_115337894delinsTG	NCBI36
NG_008956.1:g.40126_40127delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-61_1519-60delinsTG MANE Select	ENSP00000277903.4:n.1519-61_1519-60delinsTG
ENST00000351270.3:c.1519-61_1519-60delinsTG	ENSP00000277903.4:n.1519-61_1519-60delinsTG
ENST00000542051.5:c.1441-61_1441-60delinsTG	ENSP00000443283.1:n.1441-61_1441-60delinsTG
NM_001177660.1:c.1441-61_1441-60delinsTG	NP_001171131.1:n.1441-61_1441-60delinsTG
NM_004132.3:c.1519-61_1519-60delinsTG	NP_004123.1:n.1519-61_1519-60delinsTG
NM_001177660.2:c.1441-61_1441-60delinsTG	NP_001171131.1:n.1441-61_1441-60delinsTG
NM_004132.4:c.1519-61_1519-60delinsTG	NP_004123.1:n.1519-61_1519-60delinsTG
NM_004132.5:c.1519-61_1519-60delinsTG MANE Select	NP_004123.1:n.1519-61_1519-60delinsTG
NM_001177660.3:c.1441-61_1441-60delinsTG	NP_001171131.1:n.1441-61_1441-60delinsTG