Canonical Allele Identifier: CA2566260562

Gene: AMMECR1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.110264408_110264409insGGAAA , CM000685.2:g.110264408_110264409insGGAAA	GRCh38
NC_000023.10:g.109507636_109507637insGGAAA , CM000685.1:g.109507636_109507637insGGAAA	GRCh37
NC_000023.9:g.109394292_109394293insGGAAA	NCBI36
NG_016469.1:g.180828_180829insCCTTT
NG_016469.2:g.180828_180829insCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686065.1:c.584+83_584+84insCCTTT	ENSP00000509935.1:n.584+83_584+84insCCTTT
ENST00000262844.10:c.584+83_584+84insCCTTT MANE Select	ENSP00000262844.5:n.584+83_584+84insCCTTT
ENST00000680410.1:n.551+83_551+84insCCTTT
ENST00000262844.9:c.584+83_584+84insCCTTT	ENSP00000262844.5:n.584+83_584+84insCCTTT
ENST00000372057.1:c.215+83_215+84insCCTTT	ENSP00000361127.1:n.215+83_215+84insCCTTT
ENST00000372059.6:c.474-47774_474-47773insCCTTT	ENSP00000361129.2:n.474-47774_474-47773insCCTTT
ENST00000473662.1:n.284+83_284+84insCCTTT
NM_001025580.1:c.474-47774_474-47773insCCTTT	NP_001020751.1:n.474-47774_474-47773insCCTTT
NM_001171689.1:c.215+83_215+84insCCTTT	NP_001165160.1:n.215+83_215+84insCCTTT
NM_015365.2:c.584+83_584+84insCCTTT	NP_056180.1:n.584+83_584+84insCCTTT
NM_015365.3:c.584+83_584+84insCCTTT MANE Select	NP_056180.1:n.584+83_584+84insCCTTT
NM_001025580.2:c.474-47774_474-47773insCCTTT	NP_001020751.1:n.474-47774_474-47773insCCTTT
NM_001171689.2:c.215+83_215+84insCCTTT	NP_001165160.1:n.215+83_215+84insCCTTT