Canonical Allele Identifier: CA2838434195

Gene: PRR29 ICAM2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64002994G>C , CM000679.2:g.64002994G>C	GRCh38
NC_000017.10:g.62080354G>C , CM000679.1:g.62080354G>C	GRCh37
NC_000017.9:g.59434086G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412177.6:c.*1233G>C (PRR29) MANE Select	ENSP00000400986.1:n.*1233G>C
ENST00000579788.6:c.650-69C>G (ICAM2) MANE Select	ENSP00000464665.1:n.650-69C>G
ENST00000225760.5:n.1768G>C (PRR29)
ENST00000412177.5:c.*1233G>C (PRR29)	ENSP00000400986.1:n.*1233G>C
ENST00000412356.5:c.650-69C>G (ICAM2)	ENSP00000415283.1:n.650-69C>G
ENST00000418105.5:c.650-69C>G (ICAM2)	ENSP00000388666.1:n.650-69C>G
ENST00000449662.6:c.650-69C>G (ICAM2)	ENSP00000392634.2:n.650-69C>G
ENST00000578379.5:c.347-69C>G (ICAM2)	ENSP00000463199.1:n.347-69C>G
ENST00000578892.5:c.578-69C>G (ICAM2)	ENSP00000464372.1:n.578-69C>G
ENST00000579687.5:c.650-69C>G (ICAM2)	ENSP00000462579.1:n.650-69C>G
ENST00000579788.5:c.650-69C>G (ICAM2)	ENSP00000464665.1:n.650-69C>G
ENST00000581417.5:n.821-69C>G (ICAM2)
ENST00000582530.5:n.1998G>C (PRR29)
ENST00000583684.5:c.*252-69C>G (ICAM2)	ENSP00000462617.1:n.*252-69C>G
NM_000873.3:c.650-69C>G (ICAM2)	NP_000864.2:n.650-69C>G
NM_001099786.1:c.650-69C>G (ICAM2)	NP_001093256.1:n.650-69C>G
NM_001099787.1:c.650-69C>G (ICAM2)	NP_001093257.1:n.650-69C>G
NM_001099788.1:c.650-69C>G (ICAM2)	NP_001093258.1:n.650-69C>G
NM_001099789.1:c.650-69C>G (ICAM2)	NP_001093259.1:n.650-69C>G
NM_001164257.1:c.*1233G>C (PRR29)	NP_001157729.1:n.*1233G>C
NM_001191029.1:c.*1019G>C (PRR29)	NP_001177958.1:n.*1019G>C
NM_001191030.1:c.*1233G>C (PRR29)	NP_001177959.1:n.*1233G>C
NM_001191031.1:c.*1279G>C (PRR29)	NP_001177960.1:n.*1279G>C
XM_011525469.1:c.*1233G>C (PRR29)	XP_011523771.1:n.*1233G>C
XM_017025315.1:c.*1019G>C (PRR29)	XP_016880804.1:n.*1019G>C
NM_001099789.2:c.650-69C>G (ICAM2) MANE Select	NP_001093259.1:n.650-69C>G
NM_001164257.2:c.*1233G>C (PRR29) MANE Select	NP_001157729.1:n.*1233G>C
NM_001191029.2:c.*1019G>C (PRR29)	NP_001177958.1:n.*1019G>C
NM_001191030.2:c.*1233G>C (PRR29)	NP_001177959.1:n.*1233G>C
NM_001191031.2:c.*1279G>C (PRR29)	NP_001177960.1:n.*1279G>C
NM_000873.4:c.650-69C>G (ICAM2)	NP_000864.2:n.650-69C>G
NM_001099786.2:c.650-69C>G (ICAM2)	NP_001093256.1:n.650-69C>G
NM_001099787.2:c.650-69C>G (ICAM2)	NP_001093257.1:n.650-69C>G
NM_001099788.2:c.650-69C>G (ICAM2)	NP_001093258.1:n.650-69C>G