Canonical Allele Identifier: CA401079623

Gene: ITGB4 GALK1

Linked Data

• gnomAD v4: 17-75752256-G-C
• MyVariant Identifiers: chr17:g.73748337G>C (hg19) ; chr17:g.75752256G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75752256G>C , CM000679.2:g.75752256G>C	GRCh38
NC_000017.10:g.73748337G>C , CM000679.1:g.73748337G>C	GRCh37
NC_000017.9:g.71259932G>C	NCBI36
NG_007372.1:g.35822G>C
NG_008079.2:g.17944C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449880.7:c.3876G>C (ITGB4)	ENSP00000400217.2:p.Gln1292His
ENST00000200181.8:c.3876G>C (ITGB4) MANE Select	ENSP00000200181.3:p.Gln1292His
ENST00000200181.7:c.3876G>C (ITGB4)	ENSP00000200181.3:p.Gln1292His
ENST00000225614.6:c.*23-519C>G (GALK1)	ENSP00000225614.1:n.*23-519C>G
ENST00000449880.6:c.3876G>C (ITGB4)	ENSP00000400217.2:p.Gln1292His
ENST00000450894.7:c.3876G>C (ITGB4)	ENSP00000405536.3:p.Gln1292His
ENST00000579662.5:c.3876G>C (ITGB4)	ENSP00000463651.1:p.Gln1292His
ENST00000582629.1:c.266-5370G>C (ITGB4)	ENSP00000463788.1:n.266-5370G>C
ENST00000583327.2:n.119G>C (ITGB4)
ENST00000589643.1:n.255-519C>G (GALK1)
NM_000213.3:c.3876G>C (ITGB4)	NP_000204.3:p.Gln1292His
NM_001005619.1:c.3876G>C (ITGB4)	NP_001005619.1:p.Gln1292His
NM_001005731.1:c.3876G>C (ITGB4)	NP_001005731.1:p.Gln1292His
XM_005257309.2:c.3876G>C (ITGB4)	XP_005257366.1:p.Gln1292His
XM_005257311.3:c.3876G>C (ITGB4)	XP_005257368.1:p.Gln1292His
XM_005257312.2:c.3876G>C (ITGB4)	XP_005257369.1:p.Gln1292His
XM_006721866.2:c.3981G>C (ITGB4)	XP_006721929.1:p.Gln1327His
XM_006721867.2:c.3981G>C (ITGB4)	XP_006721930.1:p.Gln1327His
XM_006721868.2:c.3981G>C (ITGB4)	XP_006721931.1:p.Gln1327His
XM_006721870.2:c.3981G>C (ITGB4)	XP_006721933.1:p.Gln1327His
XM_011524751.1:c.3981G>C (ITGB4)	XP_011523053.1:p.Gln1327His
XM_011524752.1:c.1821G>C (ITGB4)	XP_011523054.1:p.Gln607His
NM_000213.4:c.3876G>C (ITGB4)	NP_000204.3:p.Gln1292His
NM_001005731.2:c.3876G>C (ITGB4)	NP_001005731.1:p.Gln1292His
NM_001321123.1:c.3876G>C (ITGB4)	NP_001308052.1:p.Gln1292His
XM_005257311.4:c.3876G>C (ITGB4)	XP_005257368.1:p.Gln1292His
XM_006721866.3:c.3981G>C (ITGB4)	XP_006721929.1:p.Gln1327His
XM_006721867.3:c.3981G>C (ITGB4)	XP_006721930.1:p.Gln1327His
XM_006721868.3:c.3981G>C (ITGB4)	XP_006721931.1:p.Gln1327His
XM_006721870.3:c.3981G>C (ITGB4)	XP_006721933.1:p.Gln1327His
XM_011524751.2:c.3981G>C (ITGB4)	XP_011523053.1:p.Gln1327His
XM_011524752.2:c.1821G>C (ITGB4)	XP_011523054.1:p.Gln607His
NM_000213.5:c.3876G>C (ITGB4) MANE Select	NP_000204.3:p.Gln1292His
NM_001005731.3:c.3876G>C (ITGB4)	NP_001005731.1:p.Gln1292His
NM_001321123.2:c.3876G>C (ITGB4)	NP_001308052.1:p.Gln1292His
NM_001381985.1:c.*23-519C>G (GALK1)	NP_001368914.1:n.*23-519C>G