Canonical Allele Identifier: CA380182237
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296950T>C (hg19) chr11:g.44275400T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275400T>C , CM000673.2:g.44275400T>C GRCh38
NC_000011.9:g.44296950T>C , CM000673.1:g.44296950T>C GRCh37
NC_000011.8:g.44253526T>C NCBI36
NG_015809.1:g.39767A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.725A>G MANE Select ENSP00000498217.1:p.Tyr242Cys
ENST00000329255.3:c.725A>G ENSP00000332744.3:p.Tyr242Cys
NM_021926.3:c.725A>G NP_068745.2:p.Tyr242Cys
XM_011520264.1:c.725A>G XP_011518566.1:p.Tyr242Cys
XM_011520265.1:c.203A>G XP_011518567.1:p.Tyr68Cys
XM_011520266.1:c.203A>G XP_011518568.1:p.Tyr68Cys
NM_021926.4:c.725A>G MANE Select NP_068745.2:p.Tyr242Cys
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