Canonical Allele Identifier: CA440606582

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102839193A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918036A>T , CM000666.2:g.101918036A>T	GRCh38
NC_000004.11:g.102839193A>T , CM000666.1:g.102839193A>T	GRCh37
NC_000004.10:g.103058216A>T	NCBI36
NG_015824.1:g.132430A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1053A>T MANE Select	ENSP00000320509.4:p.Ala351=
ENST00000322953.8:c.1053A>T	ENSP00000320509.4:p.Ala351=
ENST00000428908.5:c.654A>T	ENSP00000412748.1:p.Ala218=
ENST00000444316.2:c.963A>T	ENSP00000388817.2:p.Ala321=
ENST00000504592.5:c.1008A>T	ENSP00000421443.1:p.Ala336=
ENST00000508653.5:c.654A>T	ENSP00000422314.1:p.Ala218=
NM_001083907.2:c.963A>T	NP_001077376.2:p.Ala321=
NM_001127507.2:c.654A>T	NP_001120979.2:p.Ala218=
NM_017935.4:c.1053A>T	NP_060405.4:p.Ala351=
XM_017008337.2:c.963A>T	XP_016863826.1:p.Ala321=
NM_017935.5:c.1053A>T MANE Select	NP_060405.5:p.Ala351=
NM_001083907.3:c.963A>T	NP_001077376.3:p.Ala321=
NM_001127507.3:c.654A>T	NP_001120979.3:p.Ala218=