Canonical Allele Identifier: CA414222974

Gene: AMMECR1

Linked Data

• MyVariant Identifiers: chrX:g.109507817C>T (hg19) ; chrX:g.110264589C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.110264589C>T , CM000685.2:g.110264589C>T	GRCh38
NC_000023.10:g.109507817C>T , CM000685.1:g.109507817C>T	GRCh37
NC_000023.9:g.109394473C>T	NCBI36
NG_016469.1:g.180645G>A
NG_016469.2:g.180645G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686065.1:c.484G>A	ENSP00000509935.1:p.Val162Ile
ENST00000262844.10:c.484G>A MANE Select	ENSP00000262844.5:p.Val162Ile
ENST00000680410.1:n.451G>A
ENST00000262844.9:c.484G>A	ENSP00000262844.5:p.Val162Ile
ENST00000372057.1:c.115G>A	ENSP00000361127.1:p.Val39Ile
ENST00000372059.6:c.474-47957G>A	ENSP00000361129.2:n.474-47957G>A
ENST00000473662.1:n.184G>A
NM_001025580.1:c.474-47957G>A	NP_001020751.1:n.474-47957G>A
NM_001171689.1:c.115G>A	NP_001165160.1:p.Val39Ile
NM_015365.2:c.484G>A	NP_056180.1:p.Val162Ile
NM_015365.3:c.484G>A MANE Select	NP_056180.1:p.Val162Ile
NM_001025580.2:c.474-47957G>A	NP_001020751.1:n.474-47957G>A
NM_001171689.2:c.115G>A	NP_001165160.1:p.Val39Ile