Canonical Allele Identifier: CA2810450867

Gene: ITGB4 GALK1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75752332_75752333insACACA , CM000679.2:g.75752332_75752333insACACA	GRCh38
NC_000017.10:g.73748413_73748414insACACA , CM000679.1:g.73748413_73748414insACACA	GRCh37
NC_000017.9:g.71260008_71260009insACACA	NCBI36
NG_007372.1:g.35898_35899insACACA
NG_008079.2:g.17869_17870insTGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449880.7:c.3952_3953insACACA (ITGB4)	ENSP00000400217.2:p.Thr1318AsnfsTer?
ENST00000200181.8:c.3952_3953insACACA (ITGB4) MANE Select	ENSP00000200181.3:p.Thr1318AsnfsTer?
ENST00000200181.7:c.3952_3953insACACA (ITGB4)	ENSP00000200181.3:p.Thr1318AsnfsTer?
ENST00000225614.6:c.*23-594_*23-593insTGTTG (GALK1)	ENSP00000225614.1:n.*23-594_*23-593insTGTTG
ENST00000449880.6:c.3952_3953insACACA (ITGB4)	ENSP00000400217.2:p.Thr1318AsnfsTer?
ENST00000450894.7:c.3952_3953insACACA (ITGB4)	ENSP00000405536.3:p.Thr1318AsnfsTer?
ENST00000579662.5:c.3952_3953insACACA (ITGB4)	ENSP00000463651.1:p.Thr1318AsnfsTer?
ENST00000582629.1:c.266-5294_266-5293insACACA (ITGB4)	ENSP00000463788.1:n.266-5294_266-5293insACACA
ENST00000583327.2:n.195_196insACACA (ITGB4)
ENST00000589643.1:n.255-594_255-593insTGTTG (GALK1)
NM_000213.3:c.3952_3953insACACA (ITGB4)	NP_000204.3:p.Thr1318AsnfsTer?
NM_001005619.1:c.3952_3953insACACA (ITGB4)	NP_001005619.1:p.Thr1318AsnfsTer?
NM_001005731.1:c.3952_3953insACACA (ITGB4)	NP_001005731.1:p.Thr1318AsnfsTer?
XM_005257309.2:c.3952_3953insACACA (ITGB4)	XP_005257366.1:p.Thr1318AsnfsTer?
XM_005257311.3:c.3952_3953insACACA (ITGB4)	XP_005257368.1:p.Thr1318AsnfsTer?
XM_005257312.2:c.3952_3953insACACA (ITGB4)	XP_005257369.1:p.Thr1318AsnfsTer?
XM_006721866.2:c.4057_4058insACACA (ITGB4)	XP_006721929.1:p.Thr1353AsnfsTer?
XM_006721867.2:c.4057_4058insACACA (ITGB4)	XP_006721930.1:p.Thr1353AsnfsTer?
XM_006721868.2:c.4057_4058insACACA (ITGB4)	XP_006721931.1:p.Thr1353AsnfsTer?
XM_006721870.2:c.4057_4058insACACA (ITGB4)	XP_006721933.1:p.Thr1353AsnfsTer?
XM_011524751.1:c.4057_4058insACACA (ITGB4)	XP_011523053.1:p.Thr1353AsnfsTer?
XM_011524752.1:c.1897_1898insACACA (ITGB4)	XP_011523054.1:p.Thr633AsnfsTer?
NM_000213.4:c.3952_3953insACACA (ITGB4)	NP_000204.3:p.Thr1318AsnfsTer?
NM_001005731.2:c.3952_3953insACACA (ITGB4)	NP_001005731.1:p.Thr1318AsnfsTer?
NM_001321123.1:c.3952_3953insACACA (ITGB4)	NP_001308052.1:p.Thr1318AsnfsTer?
XM_005257311.4:c.3952_3953insACACA (ITGB4)	XP_005257368.1:p.Thr1318AsnfsTer?
XM_006721866.3:c.4057_4058insACACA (ITGB4)	XP_006721929.1:p.Thr1353AsnfsTer?
XM_006721867.3:c.4057_4058insACACA (ITGB4)	XP_006721930.1:p.Thr1353AsnfsTer?
XM_006721868.3:c.4057_4058insACACA (ITGB4)	XP_006721931.1:p.Thr1353AsnfsTer?
XM_006721870.3:c.4057_4058insACACA (ITGB4)	XP_006721933.1:p.Thr1353AsnfsTer?
XM_011524751.2:c.4057_4058insACACA (ITGB4)	XP_011523053.1:p.Thr1353AsnfsTer?
XM_011524752.2:c.1897_1898insACACA (ITGB4)	XP_011523054.1:p.Thr633AsnfsTer?
NM_000213.5:c.3952_3953insACACA (ITGB4) MANE Select	NP_000204.3:p.Thr1318AsnfsTer?
NM_001005731.3:c.3952_3953insACACA (ITGB4)	NP_001005731.1:p.Thr1318AsnfsTer?
NM_001321123.2:c.3952_3953insACACA (ITGB4)	NP_001308052.1:p.Thr1318AsnfsTer?
NM_001381985.1:c.*23-594_*23-593insTGTTG (GALK1)	NP_001368914.1:n.*23-594_*23-593insTGTTG