Canonical Allele Identifier: CA1140543122

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047825_1047826delinsCC , CM000663.2:g.1047825_1047826delinsCC	GRCh38
NC_000001.10:g.983205_983206delinsCC , CM000663.1:g.983205_983206delinsCC	GRCh37
NC_000001.9:g.973068_973069delinsCC	NCBI36
NG_016346.1:g.32703_32704delinsCC , LRG_198:g.32703_32704delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3681_3682delinsCC MANE Select	ENSP00000368678.2:p.Ile1227=
ENST00000651234.1:c.3366_3367delinsCC	ENSP00000499046.1:p.Ile1122=
ENST00000652369.1:c.3366_3367delinsCC	ENSP00000498543.1:p.Ile1122=
ENST00000379370.6:c.3681_3682delinsCC	ENSP00000368678.2:p.Ile1227=
ENST00000466223.1:n.419_420delinsCC
ENST00000478677.1:n.263_264delinsCC
ENST00000620552.4:c.3267_3268delinsCC	ENSP00000484607.1:p.Ile1089=
NM_001305275.1:c.3681_3682delinsCC	NP_001292204.1:p.Ile1227=
NM_198576.3:c.3681_3682delinsCC	NP_940978.2:p.Ile1227=
XM_005244749.2:c.3681_3682delinsCC	XP_005244806.1:p.Ile1227=
XM_006710635.2:c.3681_3682delinsCC	XP_006710698.1:p.Ile1227=
XM_011541429.1:c.3681_3682delinsCC	XP_011539731.1:p.Ile1227=
XM_011541430.1:c.2808_2809delinsCC	XP_011539732.1:p.Ile936=
XM_011541431.1:c.1947_1948delinsCC	XP_011539733.1:p.Ile649=
XR_946650.1:n.3748_3749delinsCC
NM_001364727.1:c.3366_3367delinsCC	NP_001351656.1:p.Ile1122=
XM_005244749.3:c.3681_3682delinsCC	XP_005244806.1:p.Ile1227=
XM_011541429.2:c.3681_3682delinsCC	XP_011539731.1:p.Ile1227=
XR_946650.2:n.3752_3753delinsCC
NM_001305275.2:c.3681_3682delinsCC	NP_001292204.1:p.Ile1227=
NM_198576.4:c.3681_3682delinsCC MANE Select	NP_940978.2:p.Ile1227=
NM_001364727.2:c.3366_3367delinsCC	NP_001351656.1:p.Ile1122=