Canonical Allele Identifier: CA2694459765

Gene: AMMECR1

Linked Data

• gnomAD v4: X-110264657-TTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.110264658_110264659del , CM000685.2:g.110264658_110264659del	GRCh38
NC_000023.10:g.109507886_109507887del , CM000685.1:g.109507886_109507887del	GRCh37
NC_000023.9:g.109394542_109394543del	NCBI36
NG_016469.1:g.180575_180576del
NG_016469.2:g.180575_180576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686065.1:c.474-60_474-59del	ENSP00000509935.1:n.474-60_474-59del
ENST00000262844.10:c.474-60_474-59del MANE Select	ENSP00000262844.5:n.474-60_474-59del
ENST00000680410.1:n.441-60_441-59del
ENST00000262844.9:c.474-60_474-59del	ENSP00000262844.5:n.474-60_474-59del
ENST00000372057.1:c.105-60_105-59del	ENSP00000361127.1:n.105-60_105-59del
ENST00000372059.6:c.474-48027_474-48026del	ENSP00000361129.2:n.474-48027_474-48026del
ENST00000473662.1:n.174-60_174-59del
NM_001025580.1:c.474-48027_474-48026del	NP_001020751.1:n.474-48027_474-48026del
NM_001171689.1:c.105-60_105-59del	NP_001165160.1:n.105-60_105-59del
NM_015365.2:c.474-60_474-59del	NP_056180.1:n.474-60_474-59del
NM_015365.3:c.474-60_474-59del MANE Select	NP_056180.1:n.474-60_474-59del
NM_001025580.2:c.474-48027_474-48026del	NP_001020751.1:n.474-48027_474-48026del
NM_001171689.2:c.105-60_105-59del	NP_001165160.1:n.105-60_105-59del