Canonical Allele Identifier: CA518012808

Gene: AMMECR1

Linked Data

• MyVariant Identifiers: chrX:g.109507803A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.110264575A>G , CM000685.2:g.110264575A>G	GRCh38
NC_000023.10:g.109507803A>G , CM000685.1:g.109507803A>G	GRCh37
NC_000023.9:g.109394459A>G	NCBI36
NG_016469.1:g.180659T>C
NG_016469.2:g.180659T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686065.1:c.498T>C	ENSP00000509935.1:p.Ile166=
ENST00000262844.10:c.498T>C MANE Select	ENSP00000262844.5:p.Ile166=
ENST00000680410.1:n.465T>C
ENST00000262844.9:c.498T>C	ENSP00000262844.5:p.Ile166=
ENST00000372057.1:c.129T>C	ENSP00000361127.1:p.Ile43=
ENST00000372059.6:c.474-47943T>C	ENSP00000361129.2:n.474-47943T>C
ENST00000473662.1:n.198T>C
NM_001025580.1:c.474-47943T>C	NP_001020751.1:n.474-47943T>C
NM_001171689.1:c.129T>C	NP_001165160.1:p.Ile43=
NM_015365.2:c.498T>C	NP_056180.1:p.Ile166=
NM_015365.3:c.498T>C MANE Select	NP_056180.1:p.Ile166=
NM_001025580.2:c.474-47943T>C	NP_001020751.1:n.474-47943T>C
NM_001171689.2:c.129T>C	NP_001165160.1:p.Ile43=