Canonical Allele Identifier: CA401079634

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75752257C>A , CM000679.2:g.75752257C>A GRCh38
NC_000017.10:g.73748338C>A , CM000679.1:g.73748338C>A GRCh37
NC_000017.9:g.71259933C>A NCBI36
NG_007372.1:g.35823C>A
NG_008079.2:g.17943G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000449880.7:c.3877C>A (ITGB4) ENSP00000400217.2:p.Pro1293Thr
ENST00000200181.8:c.3877C>A (ITGB4) MANE Select ENSP00000200181.3:p.Pro1293Thr
ENST00000200181.7:c.3877C>A (ITGB4) ENSP00000200181.3:p.Pro1293Thr
ENST00000225614.6:c.*23-520G>T (GALK1) ENSP00000225614.1:n.*23-520G>T
ENST00000449880.6:c.3877C>A (ITGB4) ENSP00000400217.2:p.Pro1293Thr
ENST00000450894.7:c.3877C>A (ITGB4) ENSP00000405536.3:p.Pro1293Thr
ENST00000579662.5:c.3877C>A (ITGB4) ENSP00000463651.1:p.Pro1293Thr
ENST00000582629.1:c.266-5369C>A (ITGB4) ENSP00000463788.1:n.266-5369C>A
ENST00000583327.2:n.120C>A (ITGB4)
ENST00000589643.1:n.255-520G>T (GALK1)
NM_000213.3:c.3877C>A (ITGB4) NP_000204.3:p.Pro1293Thr
NM_001005619.1:c.3877C>A (ITGB4) NP_001005619.1:p.Pro1293Thr
NM_001005731.1:c.3877C>A (ITGB4) NP_001005731.1:p.Pro1293Thr
XM_005257309.2:c.3877C>A (ITGB4) XP_005257366.1:p.Pro1293Thr
XM_005257311.3:c.3877C>A (ITGB4) XP_005257368.1:p.Pro1293Thr
XM_005257312.2:c.3877C>A (ITGB4) XP_005257369.1:p.Pro1293Thr
XM_006721866.2:c.3982C>A (ITGB4) XP_006721929.1:p.Pro1328Thr
XM_006721867.2:c.3982C>A (ITGB4) XP_006721930.1:p.Pro1328Thr
XM_006721868.2:c.3982C>A (ITGB4) XP_006721931.1:p.Pro1328Thr
XM_006721870.2:c.3982C>A (ITGB4) XP_006721933.1:p.Pro1328Thr
XM_011524751.1:c.3982C>A (ITGB4) XP_011523053.1:p.Pro1328Thr
XM_011524752.1:c.1822C>A (ITGB4) XP_011523054.1:p.Pro608Thr
NM_000213.4:c.3877C>A (ITGB4) NP_000204.3:p.Pro1293Thr
NM_001005731.2:c.3877C>A (ITGB4) NP_001005731.1:p.Pro1293Thr
NM_001321123.1:c.3877C>A (ITGB4) NP_001308052.1:p.Pro1293Thr
XM_005257311.4:c.3877C>A (ITGB4) XP_005257368.1:p.Pro1293Thr
XM_006721866.3:c.3982C>A (ITGB4) XP_006721929.1:p.Pro1328Thr
XM_006721867.3:c.3982C>A (ITGB4) XP_006721930.1:p.Pro1328Thr
XM_006721868.3:c.3982C>A (ITGB4) XP_006721931.1:p.Pro1328Thr
XM_006721870.3:c.3982C>A (ITGB4) XP_006721933.1:p.Pro1328Thr
XM_011524751.2:c.3982C>A (ITGB4) XP_011523053.1:p.Pro1328Thr
XM_011524752.2:c.1822C>A (ITGB4) XP_011523054.1:p.Pro608Thr
NM_000213.5:c.3877C>A (ITGB4) MANE Select NP_000204.3:p.Pro1293Thr
NM_001005731.3:c.3877C>A (ITGB4) NP_001005731.1:p.Pro1293Thr
NM_001321123.2:c.3877C>A (ITGB4) NP_001308052.1:p.Pro1293Thr
NM_001381985.1:c.*23-520G>T (GALK1) NP_001368914.1:n.*23-520G>T