Canonical Allele Identifier: CA8770397

Gene: ITGB4 GALK1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75756819C>T , CM000679.2:g.75756819C>T	GRCh38
NC_000017.10:g.73752900C>T , CM000679.1:g.73752900C>T	GRCh37
NC_000017.9:g.71264495C>T	NCBI36
NG_007372.1:g.40385C>T
NG_008079.1:g.13381G>A
NG_008079.2:g.13381G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449880.7:c.4962C>T (ITGB4)	ENSP00000400217.2:p.Ile1654=
ENST00000200181.8:c.5013C>T (ITGB4) MANE Select	ENSP00000200181.3:p.Ile1671=
ENST00000200181.7:c.5013C>T (ITGB4)	ENSP00000200181.3:p.Ile1671=
ENST00000225614.6:c.*22+1215G>A (GALK1)	ENSP00000225614.1:n.*22+1215G>A
ENST00000449880.6:c.4962C>T (ITGB4)	ENSP00000400217.2:p.Ile1654=
ENST00000450894.7:c.4803C>T (ITGB4)	ENSP00000405536.3:p.Ile1601=
ENST00000579662.5:c.4803C>T (ITGB4)	ENSP00000463651.1:p.Ile1601=
ENST00000582629.1:c.266-807C>T (ITGB4)	ENSP00000463788.1:n.266-807C>T
ENST00000584939.1:c.503C>T (ITGB4)
ENST00000589643.1:n.254+1215G>A (GALK1)
NM_000213.3:c.5013C>T (ITGB4)	NP_000204.3:p.Ile1671=
NM_001005619.1:c.4962C>T (ITGB4)	NP_001005619.1:p.Ile1654=
NM_001005731.1:c.4803C>T (ITGB4)	NP_001005731.1:p.Ile1601=
XM_005257309.2:c.5172C>T (ITGB4)	XP_005257366.1:p.Ile1724=
XM_005257311.3:c.5172C>T (ITGB4)	XP_005257368.1:p.Ile1724=
XM_005257312.2:c.4803C>T (ITGB4)	XP_005257369.1:p.Ile1601=
XM_006721866.2:c.5277C>T (ITGB4)	XP_006721929.1:p.Ile1759=
XM_006721867.2:c.5118C>T (ITGB4)	XP_006721930.1:p.Ile1706=
XM_006721868.2:c.5067C>T (ITGB4)	XP_006721931.1:p.Ile1689=
XM_006721870.2:c.4908C>T (ITGB4)	XP_006721933.1:p.Ile1636=
XM_011524751.1:c.4968C>T (ITGB4)	XP_011523053.1:p.Ile1656=
XM_011524752.1:c.3117C>T (ITGB4)	XP_011523054.1:p.Ile1039=
NM_000213.4:c.5013C>T (ITGB4)	NP_000204.3:p.Ile1671=
NM_001005731.2:c.4803C>T (ITGB4)	NP_001005731.1:p.Ile1601=
NM_001321123.1:c.4803C>T (ITGB4)	NP_001308052.1:p.Ile1601=
XM_005257311.4:c.5172C>T (ITGB4)	XP_005257368.1:p.Ile1724=
XM_006721866.3:c.5277C>T (ITGB4)	XP_006721929.1:p.Ile1759=
XM_006721867.3:c.5118C>T (ITGB4)	XP_006721930.1:p.Ile1706=
XM_006721868.3:c.5067C>T (ITGB4)	XP_006721931.1:p.Ile1689=
XM_006721870.3:c.4908C>T (ITGB4)	XP_006721933.1:p.Ile1636=
XM_011524751.2:c.4968C>T (ITGB4)	XP_011523053.1:p.Ile1656=
XM_011524752.2:c.3117C>T (ITGB4)	XP_011523054.1:p.Ile1039=
NM_000213.5:c.5013C>T (ITGB4) MANE Select	NP_000204.3:p.Ile1671=
NM_001005731.3:c.4803C>T (ITGB4)	NP_001005731.1:p.Ile1601=
NM_001321123.2:c.4803C>T (ITGB4)	NP_001308052.1:p.Ile1601=
NM_001381985.1:c.*22+1215G>A (GALK1)	NP_001368914.1:n.*22+1215G>A