Canonical Allele Identifier: CA2195282934
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90766922_90766928delinsTATCTGA , CM000677.2:g.90766922_90766928delinsTATCTGA GRCh38
NC_000015.9:g.91310152_91310158delinsTATCTGA , CM000677.1:g.91310152_91310158delinsTATCTGA GRCh37
NC_000015.8:g.89111156_89111162delinsTATCTGA NCBI36
NG_007272.1:g.54551_54557delinsTATCTGA , LRG_20:g.54551_54557delinsTATCTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.2206_2212delinsTATCTGA MANE Select ENSP00000347232.3:p.Tyr736=
ENST00000648453.1:c.2206_2212delinsTATCTGA ENSP00000497646.1:p.Tyr736=
ENST00000680772.1:c.2206_2212delinsTATCTGA ENSP00000506117.1:p.Tyr736=
ENST00000681142.1:c.2206_2212delinsTATCTGA ENSP00000506682.1:p.Tyr736=
ENST00000355112.7:c.2206_2212delinsTATCTGA ENSP00000347232.3:p.Tyr736=
ENST00000559426.5:n.383_389delinsTATCTGA
ENST00000559724.5:c.*1130_*1136delinsTATCTGA ENSP00000453359.1:n.*1130_*1136delinsTATC...
ENST00000560136.5:n.232_238delinsTATCTGA
ENST00000560509.5:c.2206_2212delinsTATCTGA ENSP00000454158.1:p.Tyr736=
NM_000057.3:c.2206_2212delinsTATCTGA NP_000048.1:p.Tyr736=
NM_001287246.1:c.2206_2212delinsTATCTGA NP_001274175.1:p.Tyr736=
NM_001287247.1:c.2206_2212delinsTATCTGA NP_001274176.1:p.Tyr736=
NM_001287248.1:c.1081_1087delinsTATCTGA NP_001274177.1:p.Tyr361=
XM_006720632.2:c.244_250delinsTATCTGA XP_006720695.1:p.Tyr82=
XM_011521881.1:c.892_898delinsTATCTGA XP_011520183.1:p.Tyr298=
XM_011521882.1:c.2206_2212delinsTATCTGA XP_011520184.1:p.Tyr736=
XM_011521881.2:c.892_898delinsTATCTGA XP_011520183.1:p.Tyr298=
XM_011521882.3:c.2206_2212delinsTATCTGA XP_011520184.1:p.Tyr736=
NM_000057.4:c.2206_2212delinsTATCTGA MANE Select NP_000048.1:p.Tyr736=
NM_001287246.2:c.2206_2212delinsTATCTGA NP_001274175.1:p.Tyr736=
NM_001287247.2:c.2206_2212delinsTATCTGA NP_001274176.1:p.Tyr736=
NM_001287248.2:c.1081_1087delinsTATCTGA NP_001274177.1:p.Tyr361=