Canonical Allele Identifier: CA8768901

Gene: ITGB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75731354C>T , CM000679.2:g.75731354C>T	GRCh38
NC_000017.10:g.73727435C>T , CM000679.1:g.73727435C>T	GRCh37
NC_000017.9:g.71239030C>T	NCBI36
NG_007372.1:g.14920C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449880.7:c.1201C>T	ENSP00000400217.2:p.Arg401Trp
ENST00000200181.8:c.1201C>T MANE Select	ENSP00000200181.3:p.Arg401Trp
ENST00000200181.7:c.1201C>T	ENSP00000200181.3:p.Arg401Trp
ENST00000449880.6:c.1201C>T	ENSP00000400217.2:p.Arg401Trp
ENST00000450894.7:c.1201C>T	ENSP00000405536.3:p.Arg401Trp
ENST00000579662.5:c.1201C>T	ENSP00000463651.1:p.Arg401Trp
ENST00000580542.5:n.1266C>T
ENST00000582629.1:c.265+1977C>T	ENSP00000463788.1:n.265+1977C>T
ENST00000584558.5:n.1201C>T
NM_000213.3:c.1201C>T	NP_000204.3:p.Arg401Trp
NM_001005619.1:c.1201C>T	NP_001005619.1:p.Arg401Trp
NM_001005731.1:c.1201C>T	NP_001005731.1:p.Arg401Trp
XM_005257309.2:c.1201C>T	XP_005257366.1:p.Arg401Trp
XM_005257311.3:c.1201C>T	XP_005257368.1:p.Arg401Trp
XM_005257312.2:c.1201C>T	XP_005257369.1:p.Arg401Trp
XM_006721866.2:c.1306C>T	XP_006721929.1:p.Arg436Trp
XM_006721867.2:c.1306C>T	XP_006721930.1:p.Arg436Trp
XM_006721868.2:c.1306C>T	XP_006721931.1:p.Arg436Trp
XM_006721870.2:c.1306C>T	XP_006721933.1:p.Arg436Trp
XM_011524751.1:c.1306C>T	XP_011523053.1:p.Arg436Trp
NM_000213.4:c.1201C>T	NP_000204.3:p.Arg401Trp
NM_001005731.2:c.1201C>T	NP_001005731.1:p.Arg401Trp
NM_001321123.1:c.1201C>T	NP_001308052.1:p.Arg401Trp
XM_005257311.4:c.1201C>T	XP_005257368.1:p.Arg401Trp
XM_006721866.3:c.1306C>T	XP_006721929.1:p.Arg436Trp
XM_006721867.3:c.1306C>T	XP_006721930.1:p.Arg436Trp
XM_006721868.3:c.1306C>T	XP_006721931.1:p.Arg436Trp
XM_006721870.3:c.1306C>T	XP_006721933.1:p.Arg436Trp
XM_011524751.2:c.1306C>T	XP_011523053.1:p.Arg436Trp
NM_000213.5:c.1201C>T MANE Select	NP_000204.3:p.Arg401Trp
NM_001005731.3:c.1201C>T	NP_001005731.1:p.Arg401Trp
NM_001321123.2:c.1201C>T	NP_001308052.1:p.Arg401Trp