Canonical Allele Identifier: CA8770459

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75756981G>A , CM000679.2:g.75756981G>A GRCh38
NC_000017.10:g.73753062G>A , CM000679.1:g.73753062G>A GRCh37
NC_000017.9:g.71264657G>A NCBI36
NG_007372.1:g.40547G>A
NG_008079.1:g.13219C>T
NG_008079.2:g.13219C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000449880.7:c.5041G>A (ITGB4) ENSP00000400217.2:p.Glu1681Lys
ENST00000200181.8:c.5092G>A (ITGB4) MANE Select ENSP00000200181.3:p.Glu1698Lys
ENST00000200181.7:c.5092G>A (ITGB4) ENSP00000200181.3:p.Glu1698Lys
ENST00000225614.6:c.*22+1053C>T (GALK1) ENSP00000225614.1:n.*22+1053C>T
ENST00000449880.6:c.5041G>A (ITGB4) ENSP00000400217.2:p.Glu1681Lys
ENST00000450894.7:c.4882G>A (ITGB4) ENSP00000405536.3:p.Glu1628Lys
ENST00000579662.5:c.4882G>A (ITGB4) ENSP00000463651.1:p.Glu1628Lys
ENST00000582629.1:c.266-645G>A (ITGB4) ENSP00000463788.1:n.266-645G>A
ENST00000584939.1:c.582G>A (ITGB4)
ENST00000589643.1:n.254+1053C>T (GALK1)
NM_000213.3:c.5092G>A (ITGB4) NP_000204.3:p.Glu1698Lys
NM_001005619.1:c.5041G>A (ITGB4) NP_001005619.1:p.Glu1681Lys
NM_001005731.1:c.4882G>A (ITGB4) NP_001005731.1:p.Glu1628Lys
XM_005257309.2:c.5251G>A (ITGB4) XP_005257366.1:p.Glu1751Lys
XM_005257311.3:c.5251G>A (ITGB4) XP_005257368.1:p.Glu1751Lys
XM_005257312.2:c.4882G>A (ITGB4) XP_005257369.1:p.Glu1628Lys
XM_006721866.2:c.5356G>A (ITGB4) XP_006721929.1:p.Glu1786Lys
XM_006721867.2:c.5197G>A (ITGB4) XP_006721930.1:p.Glu1733Lys
XM_006721868.2:c.5146G>A (ITGB4) XP_006721931.1:p.Glu1716Lys
XM_006721870.2:c.4987G>A (ITGB4) XP_006721933.1:p.Glu1663Lys
XM_011524751.1:c.5047G>A (ITGB4) XP_011523053.1:p.Glu1683Lys
XM_011524752.1:c.3196G>A (ITGB4) XP_011523054.1:p.Glu1066Lys
NM_000213.4:c.5092G>A (ITGB4) NP_000204.3:p.Glu1698Lys
NM_001005731.2:c.4882G>A (ITGB4) NP_001005731.1:p.Glu1628Lys
NM_001321123.1:c.4882G>A (ITGB4) NP_001308052.1:p.Glu1628Lys
XM_005257311.4:c.5251G>A (ITGB4) XP_005257368.1:p.Glu1751Lys
XM_006721866.3:c.5356G>A (ITGB4) XP_006721929.1:p.Glu1786Lys
XM_006721867.3:c.5197G>A (ITGB4) XP_006721930.1:p.Glu1733Lys
XM_006721868.3:c.5146G>A (ITGB4) XP_006721931.1:p.Glu1716Lys
XM_006721870.3:c.4987G>A (ITGB4) XP_006721933.1:p.Glu1663Lys
XM_011524751.2:c.5047G>A (ITGB4) XP_011523053.1:p.Glu1683Lys
XM_011524752.2:c.3196G>A (ITGB4) XP_011523054.1:p.Glu1066Lys
NM_000213.5:c.5092G>A (ITGB4) MANE Select NP_000204.3:p.Glu1698Lys
NM_001005731.3:c.4882G>A (ITGB4) NP_001005731.1:p.Glu1628Lys
NM_001321123.2:c.4882G>A (ITGB4) NP_001308052.1:p.Glu1628Lys
NM_001381985.1:c.*22+1053C>T (GALK1) NP_001368914.1:n.*22+1053C>T