Canonical Allele Identifier: CA414222993

Gene: AMMECR1

Linked Data

• gnomAD v4: X-110264598-G-T
• MyVariant Identifiers: chrX:g.109507826G>T (hg19) ; chrX:g.110264598G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.110264598G>T , CM000685.2:g.110264598G>T	GRCh38
NC_000023.10:g.109507826G>T , CM000685.1:g.109507826G>T	GRCh37
NC_000023.9:g.109394482G>T	NCBI36
NG_016469.1:g.180636C>A
NG_016469.2:g.180636C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686065.1:c.475C>A	ENSP00000509935.1:p.Pro159Thr
ENST00000262844.10:c.475C>A MANE Select	ENSP00000262844.5:p.Pro159Thr
ENST00000680410.1:n.442C>A
ENST00000262844.9:c.475C>A	ENSP00000262844.5:p.Pro159Thr
ENST00000372057.1:c.106C>A	ENSP00000361127.1:p.Pro36Thr
ENST00000372059.6:c.474-47966C>A	ENSP00000361129.2:n.474-47966C>A
ENST00000473662.1:n.175C>A
NM_001025580.1:c.474-47966C>A	NP_001020751.1:n.474-47966C>A
NM_001171689.1:c.106C>A	NP_001165160.1:p.Pro36Thr
NM_015365.2:c.475C>A	NP_056180.1:p.Pro159Thr
NM_015365.3:c.475C>A MANE Select	NP_056180.1:p.Pro159Thr
NM_001025580.2:c.474-47966C>A	NP_001020751.1:n.474-47966C>A
NM_001171689.2:c.106C>A	NP_001165160.1:p.Pro36Thr