Canonical Allele Identifier: CA5623426

Gene: BLNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.96216739C>G , CM000672.2:g.96216739C>G	GRCh38
NC_000010.10:g.97976495C>G , CM000672.1:g.97976495C>G	GRCh37
NC_000010.9:g.97966485C>G	NCBI36
NG_007575.1:g.64832G>C , LRG_21:g.64832G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371176.7:c.526-5G>C	ENSP00000360218.2:n.526-5G>C
ENST00000467799.7:c.350-5G>C	ENSP00000466331.3:n.350-5G>C
ENST00000472763.2:n.618-5G>C
ENST00000696248.1:c.362-6832G>C	ENSP00000512505.1:n.362-6832G>C
ENST00000696253.1:c.526-5G>C	ENSP00000512506.1:n.526-5G>C
ENST00000696255.1:c.164-5G>C	ENSP00000512507.1:n.164-5G>C
ENST00000696257.1:c.*258-5G>C	ENSP00000512509.1:n.*258-5G>C
ENST00000696513.1:c.526-5G>C	ENSP00000512679.1:n.526-5G>C
ENST00000696514.1:c.514-5G>C	ENSP00000512680.1:n.514-5G>C
ENST00000696516.1:c.367-5G>C	ENSP00000512681.1:n.367-5G>C
ENST00000696517.1:c.362-5G>C	ENSP00000512682.1:n.362-5G>C
ENST00000696518.1:c.526-5G>C	ENSP00000512683.1:n.526-5G>C
ENST00000696519.1:c.476-5G>C	ENSP00000512684.1:n.476-5G>C
ENST00000696521.1:c.476-5G>C	ENSP00000512685.1:n.476-5G>C
ENST00000696522.1:c.435-5G>C	ENSP00000512686.1:n.435-5G>C
ENST00000696523.1:c.476-5G>C	ENSP00000512687.1:n.476-5G>C
ENST00000696524.1:c.*426-5G>C	ENSP00000512688.1:n.*426-5G>C
ENST00000224337.10:c.526-5G>C MANE Select	ENSP00000224337.6:n.526-5G>C
ENST00000224337.9:c.526-5G>C	ENSP00000224337.5:n.526-5G>C
ENST00000371176.6:c.526-5G>C	ENSP00000360218.2:n.526-5G>C
ENST00000413476.6:c.526-5G>C	ENSP00000397487.2:n.526-5G>C
ENST00000427367.6:c.350-1407G>C	ENSP00000391924.3:n.350-1407G>C
ENST00000467799.6:c.362-5G>C	ENSP00000466331.2:n.362-5G>C
ENST00000472763.1:n.253-5G>C
NM_001114094.1:c.526-5G>C	NP_001107566.1:n.526-5G>C
NM_001258440.1:c.526-5G>C	NP_001245369.1:n.526-5G>C
NM_001258441.1:c.526-5G>C	NP_001245370.1:n.526-5G>C
NM_001258442.1:c.350-1407G>C	NP_001245371.1:n.350-1407G>C
NM_013314.3:c.526-5G>C , LRG_21t1:c.526-5G>C	NP_037446.1:n.526-5G>C
NR_047680.1:n.468-5G>C
NR_047681.1:n.485-5G>C
NR_047682.1:n.480-5G>C
NR_047683.1:n.644-5G>C
XM_011539728.1:c.526-5G>C	XP_011538030.1:n.526-5G>C
XM_011539728.2:c.526-5G>C	XP_011538030.1:n.526-5G>C
XM_017016159.1:c.526-5G>C	XP_016871648.1:n.526-5G>C
NM_013314.4:c.526-5G>C MANE Select	NP_037446.1:n.526-5G>C
NM_001114094.2:c.526-5G>C	NP_001107566.1:n.526-5G>C
NM_001258440.2:c.526-5G>C	NP_001245369.1:n.526-5G>C
NM_001258441.2:c.526-5G>C	NP_001245370.1:n.526-5G>C
NM_001258442.2:c.350-1407G>C	NP_001245371.1:n.350-1407G>C
NR_047680.2:n.521-5G>C
NR_047681.2:n.538-5G>C
NR_047682.2:n.533-5G>C
NR_047683.2:n.697-5G>C