Canonical Allele Identifier: CA8769872

Gene: ITGB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75750796C>T , CM000679.2:g.75750796C>T	GRCh38
NC_000017.10:g.73746877C>T , CM000679.1:g.73746877C>T	GRCh37
NC_000017.9:g.71258472C>T	NCBI36
NG_007372.1:g.34362C>T
NG_008079.2:g.19404G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000213.5:c.3591C>T MANE Select	NP_000204.3:p.Cys1197=
ENST00000200181.8:c.3591C>T MANE Select	ENSP00000200181.3:p.Cys1197=
NM_000213.3:c.3591C>T	NP_000204.3:p.Cys1197=
NM_000213.4:c.3591C>T	NP_000204.3:p.Cys1197=
NM_001005619.1:c.3591C>T	NP_001005619.1:p.Cys1197=
NM_001005731.1:c.3591C>T	NP_001005731.1:p.Cys1197=
NM_001005731.2:c.3591C>T	NP_001005731.1:p.Cys1197=
NM_001005731.3:c.3591C>T	NP_001005731.1:p.Cys1197=
NM_001321123.1:c.3591C>T	NP_001308052.1:p.Cys1197=
NM_001321123.2:c.3591C>T	NP_001308052.1:p.Cys1197=
ENST00000200181.7:c.3591C>T	ENSP00000200181.3:p.Cys1197=
ENST00000449880.6:c.3591C>T	ENSP00000400217.2:p.Cys1197=
ENST00000449880.7:c.3591C>T	ENSP00000400217.2:p.Cys1197=
ENST00000450894.7:c.3591C>T	ENSP00000405536.3:p.Cys1197=
ENST00000579662.5:c.3591C>T	ENSP00000463651.1:p.Cys1197=
ENST00000582629.1:c.266-6830C>T	ENSP00000463788.1:n.266-6830C>T
XM_005257309.2:c.3591C>T	XP_005257366.1:p.Cys1197=
XM_005257311.3:c.3591C>T	XP_005257368.1:p.Cys1197=
XM_005257311.4:c.3591C>T	XP_005257368.1:p.Cys1197=
XM_005257312.2:c.3591C>T	XP_005257369.1:p.Cys1197=
XM_006721866.2:c.3696C>T	XP_006721929.1:p.Cys1232=
XM_006721866.3:c.3696C>T	XP_006721929.1:p.Cys1232=
XM_006721867.2:c.3696C>T	XP_006721930.1:p.Cys1232=
XM_006721867.3:c.3696C>T	XP_006721930.1:p.Cys1232=
XM_006721868.2:c.3696C>T	XP_006721931.1:p.Cys1232=
XM_006721868.3:c.3696C>T	XP_006721931.1:p.Cys1232=
XM_006721870.2:c.3696C>T	XP_006721933.1:p.Cys1232=
XM_006721870.3:c.3696C>T	XP_006721933.1:p.Cys1232=
XM_011524751.1:c.3696C>T	XP_011523053.1:p.Cys1232=
XM_011524751.2:c.3696C>T	XP_011523053.1:p.Cys1232=
XM_011524752.1:c.1536C>T	XP_011523054.1:p.Cys512=
XM_011524752.2:c.1536C>T	XP_011523054.1:p.Cys512=