Canonical Allele Identifier: CA1229732243

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241877478_241877479delinsTG , CM000663.2:g.241877478_241877479delinsTG	GRCh38
NC_000001.10:g.242040780_242040781delinsTG , CM000663.1:g.242040780_242040781delinsTG	GRCh37
NC_000001.9:g.240107403_240107404delinsTG	NCBI36
NG_029100.1:g.34288_34289delinsTG
NG_029100.2:g.34288_34289delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000366548.8:c.1515-1271_1515-1270delinsTG MANE Select	ENSP00000355506.3:n.1515-1271_1515-1270de...
ENST00000348581.9:c.1515-1271_1515-1270delinsTG	ENSP00000311873.5:n.1515-1271_1515-1270de...
ENST00000366548.7:c.1515-1271_1515-1270delinsTG	ENSP00000355506.3:n.1515-1271_1515-1270de...
ENST00000518483.5:c.1515-1271_1515-1270delinsTG	ENSP00000430251.1:n.1515-1271_1515-1270de...
NM_003686.4:c.1515-1271_1515-1270delinsTG	NP_003677.4:n.1515-1271_1515-1270delinsTG...
NM_006027.4:c.1515-1271_1515-1270delinsTG	NP_006018.4:n.1515-1271_1515-1270delinsTG...
NM_130398.3:c.1515-1271_1515-1270delinsTG	NP_569082.2:n.1515-1271_1515-1270delinsTG...
XM_005273350.2:c.1512-1271_1512-1270delinsTG	XP_005273407.1:n.1512-1271_1512-1270delin...
XM_006711840.1:c.1515-1271_1515-1270delinsTG	XP_006711903.1:n.1515-1271_1515-1270delin...
XM_011544321.1:c.1515-1271_1515-1270delinsTG	XP_011542623.1:n.1515-1271_1515-1270delin...
XM_011544322.1:c.1515-1271_1515-1270delinsTG	XP_011542624.1:n.1515-1271_1515-1270delin...
XM_011544323.1:c.1512-1271_1512-1270delinsTG	XP_011542625.1:n.1512-1271_1512-1270delin...
XM_011544324.1:c.1395-1271_1395-1270delinsTG	XP_011542626.1:n.1395-1271_1395-1270delin...
XM_011544325.1:c.552-1271_552-1270delinsTG	XP_011542627.1:n.552-1271_552-1270delinsT...
XM_011544326.1:c.1517-1272_1517-1271delinsTG	XP_011542628.1:n.1517-1272_1517-1271delin...
XR_949162.1:n.2100-1271_2100-1270delinsTG
NM_001319224.1:c.1512-1271_1512-1270delinsTG	NP_001306153.1:n.1512-1271_1512-1270delin...
XM_006711840.2:c.1515-1271_1515-1270delinsTG	XP_006711903.1:n.1515-1271_1515-1270delin...
XM_011544321.2:c.1515-1271_1515-1270delinsTG	XP_011542623.1:n.1515-1271_1515-1270delin...
XM_011544323.2:c.1512-1271_1512-1270delinsTG	XP_011542625.1:n.1512-1271_1512-1270delin...
XM_011544324.2:c.1395-1271_1395-1270delinsTG	XP_011542626.1:n.1395-1271_1395-1270delin...
XM_011544325.2:c.552-1271_552-1270delinsTG	XP_011542627.1:n.552-1271_552-1270delinsT...
XM_017002793.2:c.1395-1271_1395-1270delinsTG	XP_016858282.1:n.1395-1271_1395-1270delin...
NM_130398.4:c.1515-1271_1515-1270delinsTG MANE Select	NP_569082.2:n.1515-1271_1515-1270delinsTG...
NM_001319224.2:c.1512-1271_1512-1270delinsTG	NP_001306153.1:n.1512-1271_1512-1270delin...