Canonical Allele Identifier: CA2739268378

Gene: ITGB4

Linked Data

• ClinVar Variation Id: 2778629
• ClinVar RCV Id: RCV003661604

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75727388_75727389del , CM000679.2:g.75727388_75727389del	GRCh38
NC_000017.10:g.73723469_73723470del , CM000679.1:g.73723469_73723470del	GRCh37
NC_000017.9:g.71235064_71235065del	NCBI36
NG_007372.1:g.10954_10955del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449880.7:c.163-16_163-15del	ENSP00000400217.2:n.163-16_163-15del
ENST00000200181.8:c.163-16_163-15del MANE Select	ENSP00000200181.3:n.163-16_163-15del
ENST00000200181.7:c.163-16_163-15del	ENSP00000200181.3:n.163-16_163-15del
ENST00000449880.6:c.163-16_163-15del	ENSP00000400217.2:n.163-16_163-15del
ENST00000450894.7:c.163-16_163-15del	ENSP00000405536.3:n.163-16_163-15del
ENST00000579662.5:c.163-16_163-15del	ENSP00000463651.1:n.163-16_163-15del
ENST00000580542.5:n.228-16_228-15del
ENST00000584558.5:n.163-16_163-15del
NM_000213.3:c.163-16_163-15del	NP_000204.3:n.163-16_163-15del
NM_001005619.1:c.163-16_163-15del	NP_001005619.1:n.163-16_163-15del
NM_001005731.1:c.163-16_163-15del	NP_001005731.1:n.163-16_163-15del
XM_005257309.2:c.163-16_163-15del	XP_005257366.1:n.163-16_163-15del
XM_005257311.3:c.163-16_163-15del	XP_005257368.1:n.163-16_163-15del
XM_005257312.2:c.163-16_163-15del	XP_005257369.1:n.163-16_163-15del
XM_006721866.2:c.268-16_268-15del	XP_006721929.1:n.268-16_268-15del
XM_006721867.2:c.268-16_268-15del	XP_006721930.1:n.268-16_268-15del
XM_006721868.2:c.268-16_268-15del	XP_006721931.1:n.268-16_268-15del
XM_006721870.2:c.268-16_268-15del	XP_006721933.1:n.268-16_268-15del
XM_011524751.1:c.268-16_268-15del	XP_011523053.1:n.268-16_268-15del
NM_000213.4:c.163-16_163-15del	NP_000204.3:n.163-16_163-15del
NM_001005731.2:c.163-16_163-15del	NP_001005731.1:n.163-16_163-15del
NM_001321123.1:c.163-16_163-15del	NP_001308052.1:n.163-16_163-15del
XM_005257311.4:c.163-16_163-15del	XP_005257368.1:n.163-16_163-15del
XM_006721866.3:c.268-16_268-15del	XP_006721929.1:n.268-16_268-15del
XM_006721867.3:c.268-16_268-15del	XP_006721930.1:n.268-16_268-15del
XM_006721868.3:c.268-16_268-15del	XP_006721931.1:n.268-16_268-15del
XM_006721870.3:c.268-16_268-15del	XP_006721933.1:n.268-16_268-15del
XM_011524751.2:c.268-16_268-15del	XP_011523053.1:n.268-16_268-15del
NM_000213.5:c.163-16_163-15del MANE Select	NP_000204.3:n.163-16_163-15del
NM_001005731.3:c.163-16_163-15del	NP_001005731.1:n.163-16_163-15del
NM_001321123.2:c.163-16_163-15del	NP_001308052.1:n.163-16_163-15del