Canonical Allele Identifier: CA2838484719

Gene: BLK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11527022C>T , CM000670.2:g.11527022C>T	GRCh38
NC_000008.10:g.11384531C>T , CM000670.1:g.11384531C>T	GRCh37
NC_000008.9:g.11421940C>T	NCBI36
NG_023543.1:g.38011C>T
NG_023543.2:g.38011C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.275-19030C>T
ENST00000696154.1:c.-90-19030C>T	ENSP00000512445.1:n.-90-19030C>T
ENST00000259089.9:c.-1-16202C>T MANE Select	ENSP00000259089.4:n.-1-16202C>T
ENST00000645242.1:c.-90-19030C>T	ENSP00000494690.1:n.-90-19030C>T
ENST00000259089.8:c.-1-16202C>T	ENSP00000259089.4:n.-1-16202C>T
ENST00000529894.1:c.-90-19030C>T	ENSP00000433663.1:n.-90-19030C>T
NM_001715.2:c.-1-16202C>T	NP_001706.2:n.-1-16202C>T
XM_011543824.1:c.-1-16202C>T	XP_011542126.1:n.-1-16202C>T
XM_011543827.1:c.-90-19030C>T	XP_011542129.1:n.-90-19030C>T
XM_011543828.1:c.-1-16202C>T	XP_011542130.1:n.-1-16202C>T
XM_011543829.1:c.-1-16202C>T	XP_011542131.1:n.-1-16202C>T
NM_001330465.1:c.-90-19030C>T	NP_001317394.1:n.-90-19030C>T
XM_011543828.3:c.-1-16202C>T	XP_011542130.1:n.-1-16202C>T
XM_011543829.3:c.-1-16202C>T	XP_011542131.1:n.-1-16202C>T
NM_001715.3:c.-1-16202C>T MANE Select	NP_001706.2:n.-1-16202C>T
NM_001330465.2:c.-90-19030C>T	NP_001317394.1:n.-90-19030C>T