Canonical Allele Identifier: CA2267812755

Gene: IGBP1C TEX14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58690592_58690593delinsAG , CM000679.2:g.58690592_58690593delinsAG	GRCh38
NC_000017.10:g.56767953_56767954delinsAG , CM000679.1:g.56767953_56767954delinsAG	GRCh37
NC_000017.9:g.54122952_54122953delinsAG	NCBI36
NG_023199.1:g.2991_2992delinsAG , LRG_314:g.2991_2992delinsAG
NG_047169.1:g.6487_6488delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583666.3:c.-231+1346_-231+1347delinsCT (IGBP1C) MANE Select	ENSP00000492384.1:n.-231+1346_-231+1347delinsCT
ENST00000349033.10:c.-2+1346_-2+1347delinsCT (TEX14) MANE Select	ENSP00000268910.8:n.-2+1346_-2+1347delinsCT
ENST00000583666.2:c.-231+1346_-231+1347delinsCT (IGBP1C)	ENSP00000492384.1:n.-231+1346_-231+1347delinsCT
ENST00000240361.12:c.-2+1346_-2+1347delinsCT (TEX14)	ENSP00000240361.8:n.-2+1346_-2+1347delinsCT
ENST00000349033.9:c.-2+1346_-2+1347delinsCT (TEX14)	ENSP00000268910.8:n.-2+1346_-2+1347delinsCT
ENST00000389934.7:c.-2+1346_-2+1347delinsCT (TEX14)	ENSP00000374584.3:n.-2+1346_-2+1347delinsCT
ENST00000582740.1:c.-2+1346_-2+1347delinsCT (TEX14)	ENSP00000463593.1:n.-2+1346_-2+1347delinsCT
NM_001201457.1:c.-2+1346_-2+1347delinsCT (TEX14)	NP_001188386.1:n.-2+1346_-2+1347delinsCT
NM_031272.4:c.-2+1346_-2+1347delinsCT (TEX14)	NP_112562.3:n.-2+1346_-2+1347delinsCT
NM_198393.3:c.-2+1346_-2+1347delinsCT (TEX14)	NP_938207.2:n.-2+1346_-2+1347delinsCT
XM_011525028.1:c.-2+1346_-2+1347delinsCT (TEX14)	XP_011523330.1:n.-2+1346_-2+1347delinsCT
XM_011525030.1:c.-2+1346_-2+1347delinsCT (TEX14)	XP_011523332.1:n.-2+1346_-2+1347delinsCT
XM_011525031.1:c.-2+1346_-2+1347delinsCT (TEX14)	XP_011523333.1:n.-2+1346_-2+1347delinsCT
XM_011525032.1:c.-2+1346_-2+1347delinsCT (TEX14)	XP_011523334.1:n.-2+1346_-2+1347delinsCT
NM_001201457.2:c.-2+1346_-2+1347delinsCT (TEX14)	NP_001188386.1:n.-2+1346_-2+1347delinsCT
NM_031272.5:c.-2+1346_-2+1347delinsCT (TEX14) MANE Select	NP_112562.3:n.-2+1346_-2+1347delinsCT
NM_198393.4:c.-2+1346_-2+1347delinsCT (TEX14)	NP_938207.2:n.-2+1346_-2+1347delinsCT
NM_001395966.1:c.-231+1346_-231+1347delinsCT (IGBP1C) MANE Select	NP_001382895.1:n.-231+1346_-231+1347delinsCT