Canonical Allele Identifier: CA2508713871

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99880556_99880557insAATGTCTACTAG , CM000663.2:g.99880556_99880557insAATGTCTACTAG	GRCh38
NC_000001.10:g.100346112_100346113insAATGTCTACTAG , CM000663.1:g.100346112_100346113insAATGTCTACTAG	GRCh37
NC_000001.9:g.100118700_100118701insAATGTCTACTAG	NCBI36
NG_012865.1:g.35473_35474insAATGTCTACTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1736-76_1736-75insAATGTCTACTAG MANE Select	ENSP00000355106.3:n.1736-76_1736-75insAATGTCTACTAG
ENST00000637337.1:n.1947-76_1947-75insAATGTCTACTAG
ENST00000294724.8:c.1736-76_1736-75insAATGTCTACTAG	ENSP00000294724.4:n.1736-76_1736-75insAATGTCTACTAG
ENST00000361302.7:c.1688-76_1688-75insAATGTCTACTAG	ENSP00000354971.3:n.1688-76_1688-75insAATGTCTACTAG
ENST00000361522.4:c.1685-76_1685-75insAATGTCTACTAG	ENSP00000354635.4:n.1685-76_1685-75insAATGTCTACTAG
ENST00000361915.7:c.1736-76_1736-75insAATGTCTACTAG	ENSP00000355106.3:n.1736-76_1736-75insAATGTCTACTAG
ENST00000370161.6:c.1688-76_1688-75insAATGTCTACTAG	ENSP00000359180.2:n.1688-76_1688-75insAATGTCTACTAG
ENST00000370163.7:c.1736-76_1736-75insAATGTCTACTAG	ENSP00000359182.3:n.1736-76_1736-75insAATGTCTACTAG
ENST00000370165.7:c.1736-76_1736-75insAATGTCTACTAG	ENSP00000359184.3:n.1736-76_1736-75insAATGTCTACTAG
NM_000028.2:c.1736-76_1736-75insAATGTCTACTAG	NP_000019.2:n.1736-76_1736-75insAATGTCTACTAG
NM_000642.2:c.1736-76_1736-75insAATGTCTACTAG	NP_000633.2:n.1736-76_1736-75insAATGTCTACTAG
NM_000643.2:c.1736-76_1736-75insAATGTCTACTAG	NP_000634.2:n.1736-76_1736-75insAATGTCTACTAG
NM_000644.2:c.1736-76_1736-75insAATGTCTACTAG	NP_000635.2:n.1736-76_1736-75insAATGTCTACTAG
NM_000645.2:c.1685-76_1685-75insAATGTCTACTAG	NP_000636.2:n.1685-76_1685-75insAATGTCTACTAG
NM_000646.2:c.1688-76_1688-75insAATGTCTACTAG	NP_000637.2:n.1688-76_1688-75insAATGTCTACTAG
XM_005270557.1:c.1736-76_1736-75insAATGTCTACTAG	XP_005270614.1:n.1736-76_1736-75insAATGTCTACTAG
XM_005270557.2:c.1736-76_1736-75insAATGTCTACTAG	XP_005270614.1:n.1736-76_1736-75insAATGTCTACTAG
XM_017000501.2:c.-5-76_-5-75insAATGTCTACTAG	XP_016855990.1:n.-5-76_-5-75insAATGTCTACTAG
NM_000642.3:c.1736-76_1736-75insAATGTCTACTAG MANE Select	NP_000633.2:n.1736-76_1736-75insAATGTCTACTAG