Canonical Allele Identifier: CA3725659
Community Standard Title: NM_025257.3(SLC44A4):c.537G>A (p.Gly179=)
Gene: SLC44A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31871554C>T , CM000668.2:g.31871554C>T GRCh38
NC_000006.11:g.31839331C>T , CM000668.1:g.31839331C>T GRCh37
NC_000006.10:g.31947310C>T NCBI36
NG_023058.1:g.12493G>A

Transcript Alleles

HGVS Amino-acid Change
NM_025257.3:c.537G>A MANE Select NP_079533.2:p.Gly179=
ENST00000229729.11:c.537G>A MANE Select ENSP00000229729.6:p.Gly179=
NM_001178044.1:c.411G>A NP_001171515.1:p.Gly137=
NM_001178044.2:c.411G>A NP_001171515.1:p.Gly137=
NM_001178045.1:c.309G>A NP_001171516.1:p.Gly103=
NM_001178045.2:c.309G>A NP_001171516.1:p.Gly103=
NM_025257.2:c.537G>A NP_079533.2:p.Gly179=
ENST00000229729.10:c.537G>A ENSP00000229729.6:p.Gly179=
ENST00000375562.8:c.411G>A ENSP00000364712.4:p.Gly137=
ENST00000414427.1:c.524G>A
ENST00000544672.5:c.309G>A ENSP00000444109.1:p.Gly103=