Canonical Allele Identifier: CA1929415

Gene: ITGB6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.160172707G>A , CM000664.2:g.160172707G>A	GRCh38
NC_000002.11:g.161029218G>A , CM000664.1:g.161029218G>A	GRCh37
NC_000002.10:g.160737464G>A	NCBI36
NG_042041.1:g.32607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283249.7:c.783C>T MANE Select	ENSP00000283249.2:p.Asp261=
ENST00000652612.1:n.226C>T
ENST00000283249.6:c.783C>T	ENSP00000283249.2:p.Asp261=
ENST00000409583.5:c.*397C>T	ENSP00000386477.1:n.*397C>T
ENST00000409872.1:c.783C>T	ENSP00000386367.1:p.Asp261=
ENST00000409967.6:c.783C>T	ENSP00000386828.2:p.Asp261=
ENST00000428609.6:c.657C>T	ENSP00000408024.2:p.Asp219=
ENST00000485635.1:n.1235C>T
ENST00000620391.4:c.498C>T	ENSP00000481183.1:p.Asp166=
NM_000888.4:c.783C>T	NP_000879.2:p.Asp261=
NM_001282353.1:c.783C>T	NP_001269282.1:p.Asp261=
NM_001282354.1:c.498C>T	NP_001269283.1:p.Asp166=
NM_001282355.1:c.783C>T	NP_001269284.1:p.Asp261=
NM_001282388.1:c.657C>T	NP_001269317.1:p.Asp219=
NM_001282389.1:c.564C>T	NP_001269318.1:p.Asp188=
NM_001282390.1:c.369C>T	NP_001269319.1:p.Asp123=
NM_000888.5:c.783C>T MANE Select	NP_000879.2:p.Asp261=
NM_001282353.2:c.783C>T	NP_001269282.1:p.Asp261=
NM_001282355.2:c.783C>T	NP_001269284.1:p.Asp261=
NM_001282388.2:c.657C>T	NP_001269317.1:p.Asp219=
NM_001282389.2:c.564C>T	NP_001269318.1:p.Asp188=
NM_001282390.2:c.369C>T	NP_001269319.1:p.Asp123=
NM_001282354.2:c.498C>T	NP_001269283.1:p.Asp166=