Canonical Allele Identifier: CA357956385

Gene: BANK1

Linked Data

• gnomAD v4: 4-101918140-C-T
• MyVariant Identifiers: chr4:g.102839297C>T (hg19) ; chr4:g.101918140C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918140C>T , CM000666.2:g.101918140C>T	GRCh38
NC_000004.11:g.102839297C>T , CM000666.1:g.102839297C>T	GRCh37
NC_000004.10:g.103058320C>T	NCBI36
NG_015824.1:g.132534C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1157C>T MANE Select	ENSP00000320509.4:p.Ala386Val
ENST00000322953.8:c.1157C>T	ENSP00000320509.4:p.Ala386Val
ENST00000428908.5:c.758C>T	ENSP00000412748.1:p.Ala253Val
ENST00000444316.2:c.1067C>T	ENSP00000388817.2:p.Ala356Val
ENST00000504592.5:c.1112C>T	ENSP00000421443.1:p.Ala371Val
ENST00000508653.5:c.758C>T	ENSP00000422314.1:p.Ala253Val
NM_001083907.2:c.1067C>T	NP_001077376.2:p.Ala356Val
NM_001127507.2:c.758C>T	NP_001120979.2:p.Ala253Val
NM_017935.4:c.1157C>T	NP_060405.4:p.Ala386Val
XM_017008337.2:c.1067C>T	XP_016863826.1:p.Ala356Val
NM_017935.5:c.1157C>T MANE Select	NP_060405.5:p.Ala386Val
NM_001083907.3:c.1067C>T	NP_001077376.3:p.Ala356Val
NM_001127507.3:c.758C>T	NP_001120979.3:p.Ala253Val