Canonical Allele Identifier: CA5623584

Gene: BLNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.96242742G>A , CM000672.2:g.96242742G>A	GRCh38
NC_000010.10:g.98002498G>A , CM000672.1:g.98002498G>A	GRCh37
NC_000010.9:g.97992488G>A	NCBI36
NG_007575.1:g.38829C>T , LRG_21:g.38829C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371176.7:c.156C>T	ENSP00000360218.2:p.Tyr52=
ENST00000467799.7:c.156C>T	ENSP00000466331.3:p.Tyr52=
ENST00000472763.2:n.248C>T
ENST00000495266.2:c.156C>T	ENSP00000465741.1:p.Tyr52=
ENST00000696248.1:c.156C>T	ENSP00000512505.1:p.Tyr52=
ENST00000696253.1:c.156C>T	ENSP00000512506.1:p.Tyr52=
ENST00000696255.1:c.156C>T	ENSP00000512507.1:p.Tyr52=
ENST00000696257.1:c.113+4242C>T	ENSP00000512509.1:n.113+4242C>T
ENST00000696513.1:c.156C>T	ENSP00000512679.1:p.Tyr52=
ENST00000696514.1:c.156C>T	ENSP00000512680.1:p.Tyr52=
ENST00000696516.1:c.156C>T	ENSP00000512681.1:p.Tyr52=
ENST00000696517.1:c.156C>T	ENSP00000512682.1:p.Tyr52=
ENST00000696518.1:c.156C>T	ENSP00000512683.1:p.Tyr52=
ENST00000696519.1:c.113+4242C>T	ENSP00000512684.1:n.113+4242C>T
ENST00000696521.1:c.113+4242C>T	ENSP00000512685.1:n.113+4242C>T
ENST00000696522.1:c.113+4242C>T	ENSP00000512686.1:n.113+4242C>T
ENST00000696523.1:c.113+4242C>T	ENSP00000512687.1:n.113+4242C>T
ENST00000696524.1:c.156C>T	ENSP00000512688.1:p.Tyr52=
ENST00000696525.1:n.276C>T
ENST00000224337.10:c.156C>T MANE Select	ENSP00000224337.6:p.Tyr52=
ENST00000224337.9:c.156C>T	ENSP00000224337.5:p.Tyr52=
ENST00000371176.6:c.156C>T	ENSP00000360218.2:p.Tyr52=
ENST00000413476.6:c.156C>T	ENSP00000397487.2:p.Tyr52=
ENST00000427367.6:c.156C>T	ENSP00000391924.3:p.Tyr52=
ENST00000467799.6:c.156C>T	ENSP00000466331.2:p.Tyr52=
ENST00000495266.1:c.156C>T	ENSP00000465741.1:p.Tyr52=
NM_001114094.1:c.156C>T	NP_001107566.1:p.Tyr52=
NM_001258440.1:c.156C>T	NP_001245369.1:p.Tyr52=
NM_001258441.1:c.156C>T	NP_001245370.1:p.Tyr52=
NM_001258442.1:c.156C>T	NP_001245371.1:p.Tyr52=
NM_013314.3:c.156C>T , LRG_21t1:c.156C>T	NP_037446.1:p.Tyr52=
NR_047680.1:n.274C>T
NR_047681.1:n.274C>T
NR_047682.1:n.274C>T
NR_047683.1:n.274C>T
XM_011539728.1:c.156C>T	XP_011538030.1:p.Tyr52=
XM_011539728.2:c.156C>T	XP_011538030.1:p.Tyr52=
XM_017016159.1:c.156C>T	XP_016871648.1:p.Tyr52=
NM_013314.4:c.156C>T MANE Select	NP_037446.1:p.Tyr52=
NM_001114094.2:c.156C>T	NP_001107566.1:p.Tyr52=
NM_001258440.2:c.156C>T	NP_001245369.1:p.Tyr52=
NM_001258441.2:c.156C>T	NP_001245370.1:p.Tyr52=
NM_001258442.2:c.156C>T	NP_001245371.1:p.Tyr52=
NR_047680.2:n.327C>T
NR_047681.2:n.327C>T
NR_047682.2:n.327C>T
NR_047683.2:n.327C>T