Canonical Allele Identifier: CA8770267
Community Standard Title: NM_000213.5(ITGB4):c.4663C>T (p.Arg1555Trp)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75755805C>T , CM000679.2:g.75755805C>T GRCh38
NC_000017.10:g.73751886C>T , CM000679.1:g.73751886C>T GRCh37
NC_000017.9:g.71263481C>T NCBI36
NG_007372.1:g.39371C>T
NG_008079.2:g.14395G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000213.5:c.4663C>T (ITGB4) MANE Select NP_000204.3:p.Arg1555Trp
ENST00000200181.8:c.4663C>T (ITGB4) MANE Select ENSP00000200181.3:p.Arg1555Trp
NM_000213.3:c.4663C>T (ITGB4) NP_000204.3:p.Arg1555Trp
NM_000213.4:c.4663C>T (ITGB4) NP_000204.3:p.Arg1555Trp
NM_001005619.1:c.4612C>T (ITGB4) NP_001005619.1:p.Arg1538Trp
NM_001005731.1:c.4453C>T (ITGB4) NP_001005731.1:p.Arg1485Trp
NM_001005731.2:c.4453C>T (ITGB4) NP_001005731.1:p.Arg1485Trp
NM_001005731.3:c.4453C>T (ITGB4) NP_001005731.1:p.Arg1485Trp
NM_001321123.1:c.4453C>T (ITGB4) NP_001308052.1:p.Arg1485Trp
NM_001321123.2:c.4453C>T (ITGB4) NP_001308052.1:p.Arg1485Trp
NM_001381985.1:c.*22+2229G>A (GALK1) NP_001368914.1:n.*22+2229G>A
ENST00000200181.7:c.4663C>T (ITGB4) ENSP00000200181.3:p.Arg1555Trp
ENST00000225614.6:c.*22+2229G>A (GALK1) ENSP00000225614.1:n.*22+2229G>A
ENST00000449880.6:c.4612C>T (ITGB4) ENSP00000400217.2:p.Arg1538Trp
ENST00000449880.7:c.4612C>T (ITGB4) ENSP00000400217.2:p.Arg1538Trp
ENST00000450894.7:c.4453C>T (ITGB4) ENSP00000405536.3:p.Arg1485Trp
ENST00000579662.5:c.4453C>T (ITGB4) ENSP00000463651.1:p.Arg1485Trp
ENST00000582629.1:c.266-1821C>T (ITGB4) ENSP00000463788.1:n.266-1821C>T
ENST00000583327.2:n.696C>T (ITGB4)
ENST00000584939.1:c.199-624C>T (ITGB4)
ENST00000589643.1:n.254+2229G>A (GALK1)
XM_005257309.2:c.4822C>T (ITGB4) XP_005257366.1:p.Arg1608Trp
XM_005257311.3:c.4822C>T (ITGB4) XP_005257368.1:p.Arg1608Trp
XM_005257311.4:c.4822C>T (ITGB4) XP_005257368.1:p.Arg1608Trp
XM_005257312.2:c.4453C>T (ITGB4) XP_005257369.1:p.Arg1485Trp
XM_006721866.2:c.4927C>T (ITGB4) XP_006721929.1:p.Arg1643Trp
XM_006721866.3:c.4927C>T (ITGB4) XP_006721929.1:p.Arg1643Trp
XM_006721867.2:c.4768C>T (ITGB4) XP_006721930.1:p.Arg1590Trp
XM_006721867.3:c.4768C>T (ITGB4) XP_006721930.1:p.Arg1590Trp
XM_006721868.2:c.4717C>T (ITGB4) XP_006721931.1:p.Arg1573Trp
XM_006721868.3:c.4717C>T (ITGB4) XP_006721931.1:p.Arg1573Trp
XM_006721870.2:c.4558C>T (ITGB4) XP_006721933.1:p.Arg1520Trp
XM_006721870.3:c.4558C>T (ITGB4) XP_006721933.1:p.Arg1520Trp
XM_011524751.1:c.4664-624C>T (ITGB4) XP_011523053.1:n.4664-624C>T
XM_011524751.2:c.4664-624C>T (ITGB4) XP_011523053.1:n.4664-624C>T
XM_011524752.1:c.2767C>T (ITGB4) XP_011523054.1:p.Arg923Trp
XM_011524752.2:c.2767C>T (ITGB4) XP_011523054.1:p.Arg923Trp