Canonical Allele Identifier: CA1937429103

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588165_113588167delinsCTG , CM000672.2:g.113588165_113588167delinsCTG	GRCh38
NC_000010.10:g.115347924_115347926delinsCTG , CM000672.1:g.115347924_115347926delinsCTG	GRCh37
NC_000010.9:g.115337914_115337916delinsCTG	NCBI36
NG_008956.1:g.40147_40149delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-40_1519-38delinsCTG MANE Select	ENSP00000277903.4:n.1519-40_1519-38delinsCTG
ENST00000351270.3:c.1519-40_1519-38delinsCTG	ENSP00000277903.4:n.1519-40_1519-38delinsCTG
ENST00000542051.5:c.1441-40_1441-38delinsCTG	ENSP00000443283.1:n.1441-40_1441-38delinsCTG
NM_001177660.1:c.1441-40_1441-38delinsCTG	NP_001171131.1:n.1441-40_1441-38delinsCTG
NM_004132.3:c.1519-40_1519-38delinsCTG	NP_004123.1:n.1519-40_1519-38delinsCTG
NM_001177660.2:c.1441-40_1441-38delinsCTG	NP_001171131.1:n.1441-40_1441-38delinsCTG
NM_004132.4:c.1519-40_1519-38delinsCTG	NP_004123.1:n.1519-40_1519-38delinsCTG
NM_004132.5:c.1519-40_1519-38delinsCTG MANE Select	NP_004123.1:n.1519-40_1519-38delinsCTG
NM_001177660.3:c.1441-40_1441-38delinsCTG	NP_001171131.1:n.1441-40_1441-38delinsCTG