Canonical Allele Identifier: CA518012823

Gene: AMMECR1

Linked Data

• MyVariant Identifiers: chrX:g.109507827G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.110264599G>A , CM000685.2:g.110264599G>A	GRCh38
NC_000023.10:g.109507827G>A , CM000685.1:g.109507827G>A	GRCh37
NC_000023.9:g.109394483G>A	NCBI36
NG_016469.1:g.180635C>T
NG_016469.2:g.180635C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686065.1:c.474C>T	ENSP00000509935.1:p.Tyr158=
ENST00000262844.10:c.474C>T MANE Select	ENSP00000262844.5:p.Tyr158=
ENST00000680410.1:n.441C>T
ENST00000262844.9:c.474C>T	ENSP00000262844.5:p.Tyr158=
ENST00000372057.1:c.105C>T	ENSP00000361127.1:p.Tyr35=
ENST00000372059.6:c.474-47967C>T	ENSP00000361129.2:n.474-47967C>T
ENST00000473662.1:n.174C>T
NM_001025580.1:c.474-47967C>T	NP_001020751.1:n.474-47967C>T
NM_001171689.1:c.105C>T	NP_001165160.1:p.Tyr35=
NM_015365.2:c.474C>T	NP_056180.1:p.Tyr158=
NM_015365.3:c.474C>T MANE Select	NP_056180.1:p.Tyr158=
NM_001025580.2:c.474-47967C>T	NP_001020751.1:n.474-47967C>T
NM_001171689.2:c.105C>T	NP_001165160.1:p.Tyr35=