Canonical Allele Identifier: CA401041535

Gene: ITGB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75729399G>T , CM000679.2:g.75729399G>T	GRCh38
NC_000017.10:g.73725480G>T , CM000679.1:g.73725480G>T	GRCh37
NC_000017.9:g.71237075G>T	NCBI36
NG_007372.1:g.12965G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000213.5:c.701G>T MANE Select	NP_000204.3:p.Gly234Val
ENST00000200181.8:c.701G>T MANE Select	ENSP00000200181.3:p.Gly234Val
NM_000213.3:c.701G>T	NP_000204.3:p.Gly234Val
NM_000213.4:c.701G>T	NP_000204.3:p.Gly234Val
NM_001005619.1:c.701G>T	NP_001005619.1:p.Gly234Val
NM_001005731.1:c.701G>T	NP_001005731.1:p.Gly234Val
NM_001005731.2:c.701G>T	NP_001005731.1:p.Gly234Val
NM_001005731.3:c.701G>T	NP_001005731.1:p.Gly234Val
NM_001321123.1:c.701G>T	NP_001308052.1:p.Gly234Val
NM_001321123.2:c.701G>T	NP_001308052.1:p.Gly234Val
ENST00000200181.7:c.701G>T	ENSP00000200181.3:p.Gly234Val
ENST00000449880.6:c.701G>T	ENSP00000400217.2:p.Gly234Val
ENST00000449880.7:c.701G>T	ENSP00000400217.2:p.Gly234Val
ENST00000450894.7:c.701G>T	ENSP00000405536.3:p.Gly234Val
ENST00000579662.5:c.701G>T	ENSP00000463651.1:p.Gly234Val
ENST00000580542.5:n.766G>T
ENST00000582629.1:c.265+22G>T	ENSP00000463788.1:n.265+22G>T
ENST00000584558.5:n.701G>T
XM_005257309.2:c.701G>T	XP_005257366.1:p.Gly234Val
XM_005257311.3:c.701G>T	XP_005257368.1:p.Gly234Val
XM_005257311.4:c.701G>T	XP_005257368.1:p.Gly234Val
XM_005257312.2:c.701G>T	XP_005257369.1:p.Gly234Val
XM_006721866.2:c.806G>T	XP_006721929.1:p.Gly269Val
XM_006721866.3:c.806G>T	XP_006721929.1:p.Gly269Val
XM_006721867.2:c.806G>T	XP_006721930.1:p.Gly269Val
XM_006721867.3:c.806G>T	XP_006721930.1:p.Gly269Val
XM_006721868.2:c.806G>T	XP_006721931.1:p.Gly269Val
XM_006721868.3:c.806G>T	XP_006721931.1:p.Gly269Val
XM_006721870.2:c.806G>T	XP_006721933.1:p.Gly269Val
XM_006721870.3:c.806G>T	XP_006721933.1:p.Gly269Val
XM_011524751.1:c.806G>T	XP_011523053.1:p.Gly269Val
XM_011524751.2:c.806G>T	XP_011523053.1:p.Gly269Val