Canonical Allele Identifier: CA392977965

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628185T>G (hg19) ; chr15:g.68335847T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335847T>G , CM000677.2:g.68335847T>G	GRCh38
NC_000015.9:g.68628185T>G , CM000677.1:g.68628185T>G	GRCh37
NC_000015.8:g.66415239T>G	NCBI36
NG_046911.1:g.101314A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-2A>C MANE Select	ENSP00000327290.7:n.1277-2A>C
ENST00000315757.8:c.1277-2A>C	ENSP00000327290.7:n.1277-2A>C
ENST00000423218.6:c.1277-2A>C	ENSP00000403392.2:n.1277-2A>C
ENST00000566429.1:n.197-33A>C
ENST00000569346.5:n.254A>C
NM_001004439.1:c.1277-2A>C	NP_001004439.1:n.1277-2A>C
XM_005254228.2:c.971-2A>C	XP_005254285.1:n.971-2A>C
XM_011521363.1:c.1070-2A>C	XP_011519665.1:n.1070-2A>C
XM_005254228.3:c.971-2A>C	XP_005254285.1:n.971-2A>C
XM_011521363.2:c.1070-2A>C	XP_011519665.1:n.1070-2A>C
NM_001004439.2:c.1277-2A>C MANE Select	NP_001004439.1:n.1277-2A>C