Canonical Allele Identifier: CA501838351

Gene: ITGB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75742632C>A , CM000679.2:g.75742632C>A	GRCh38
NC_000017.10:g.73738713C>A , CM000679.1:g.73738713C>A	GRCh37
NC_000017.9:g.71250308C>A	NCBI36
NG_007372.1:g.26198C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000213.5:c.2833C>A MANE Select	NP_000204.3:p.Arg945=
ENST00000200181.8:c.2833C>A MANE Select	ENSP00000200181.3:p.Arg945=
NM_000213.3:c.2833C>A	NP_000204.3:p.Arg945=
NM_000213.4:c.2833C>A	NP_000204.3:p.Arg945=
NM_001005619.1:c.2833C>A	NP_001005619.1:p.Arg945=
NM_001005731.1:c.2833C>A	NP_001005731.1:p.Arg945=
NM_001005731.2:c.2833C>A	NP_001005731.1:p.Arg945=
NM_001005731.3:c.2833C>A	NP_001005731.1:p.Arg945=
NM_001321123.1:c.2833C>A	NP_001308052.1:p.Arg945=
NM_001321123.2:c.2833C>A	NP_001308052.1:p.Arg945=
ENST00000200181.7:c.2833C>A	ENSP00000200181.3:p.Arg945=
ENST00000449880.6:c.2833C>A	ENSP00000400217.2:p.Arg945=
ENST00000449880.7:c.2833C>A	ENSP00000400217.2:p.Arg945=
ENST00000450894.7:c.2833C>A	ENSP00000405536.3:p.Arg945=
ENST00000579662.5:c.2833C>A	ENSP00000463651.1:p.Arg945=
ENST00000582629.1:c.265+13255C>A	ENSP00000463788.1:n.265+13255C>A
ENST00000584025.1:n.209C>A
ENST00000584558.5:n.2870C>A
XM_005257309.2:c.2833C>A	XP_005257366.1:p.Arg945=
XM_005257311.3:c.2833C>A	XP_005257368.1:p.Arg945=
XM_005257311.4:c.2833C>A	XP_005257368.1:p.Arg945=
XM_005257312.2:c.2833C>A	XP_005257369.1:p.Arg945=
XM_006721866.2:c.2938C>A	XP_006721929.1:p.Arg980=
XM_006721866.3:c.2938C>A	XP_006721929.1:p.Arg980=
XM_006721867.2:c.2938C>A	XP_006721930.1:p.Arg980=
XM_006721867.3:c.2938C>A	XP_006721930.1:p.Arg980=
XM_006721868.2:c.2938C>A	XP_006721931.1:p.Arg980=
XM_006721868.3:c.2938C>A	XP_006721931.1:p.Arg980=
XM_006721870.2:c.2938C>A	XP_006721933.1:p.Arg980=
XM_006721870.3:c.2938C>A	XP_006721933.1:p.Arg980=
XM_011524751.1:c.2938C>A	XP_011523053.1:p.Arg980=
XM_011524751.2:c.2938C>A	XP_011523053.1:p.Arg980=
XM_011524752.1:c.778C>A	XP_011523054.1:p.Arg260=
XM_011524752.2:c.778C>A	XP_011523054.1:p.Arg260=