Canonical Allele Identifier: CA1763963565

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563950_11563967delinsATGCCGCGCCCCGACACC , CM000670.2:g.11563950_11563967delinsATGCCGCGCCCCGACACC	GRCh38
NC_000008.10:g.11421459_11421476delinsATGCCGCGCCCCGACACC , CM000670.1:g.11421459_11421476delinsATGCCGCGCCCCGACACC	GRCh37
NC_000008.9:g.11458868_11458885delinsATGCCGCGCCCCGACACC	NCBI36
NG_023543.1:g.74939_74956delinsATGCCGCGCCCCGACACC
NG_023543.2:g.74939_74956delinsATGCCGCGCCCCGACACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1468_1485delinsATGCCGCGCCCCGACACC
ENST00000696154.1:c.*678_*695delinsATGCCGCGCCCCGACACC	ENSP00000512445.1:n.*678_*695delinsATGCCGCGCCCCGACACC
ENST00000696155.1:n.244_261delinsATGCCGCGCCCCGACACC
ENST00000259089.9:c.1360_1377delinsATGCCGCGCCCCGACACC MANE Select	ENSP00000259089.4:p.Met454=
ENST00000645242.1:c.1147_1164delinsATGCCGCGCCCCGACACC	ENSP00000494690.1:p.Met383=
ENST00000259089.8:c.1360_1377delinsATGCCGCGCCCCGACACC	ENSP00000259089.4:p.Met454=
ENST00000526097.1:n.1300_1317delinsATGCCGCGCCCCGACACC
ENST00000529894.1:c.1147_1164delinsATGCCGCGCCCCGACACC	ENSP00000433663.1:p.Met383=
NM_001715.2:c.1360_1377delinsATGCCGCGCCCCGACACC	NP_001706.2:p.Met454=
XM_011543824.1:c.1438_1455delinsATGCCGCGCCCCGACACC	XP_011542126.1:p.Met480=
XM_011543825.1:c.1438_1455delinsATGCCGCGCCCCGACACC	XP_011542127.1:p.Met480=
XM_011543826.1:c.1438_1455delinsATGCCGCGCCCCGACACC	XP_011542128.1:p.Met480=
XM_011543827.1:c.1225_1242delinsATGCCGCGCCCCGACACC	XP_011542129.1:p.Met409=
NM_001330465.1:c.1147_1164delinsATGCCGCGCCCCGACACC	NP_001317394.1:p.Met383=
XM_011543825.3:c.1438_1455delinsATGCCGCGCCCCGACACC	XP_011542127.1:p.Met480=
NM_001715.3:c.1360_1377delinsATGCCGCGCCCCGACACC MANE Select	NP_001706.2:p.Met454=
NM_001330465.2:c.1147_1164delinsATGCCGCGCCCCGACACC	NP_001317394.1:p.Met383=