Canonical Allele Identifier: CA2250967890
Gene: SHMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18328792G= , CM000679.2:g.18328792G= GRCh38
NC_000017.10:g.18232106G= , CM000679.1:g.18232106G= GRCh37
NC_000017.9:g.18172831G= NCBI36
NG_017111.1:g.39751C=

Transcript Alleles

HGVS Amino-acid change
ENST00000583780.2:c.1410C= ENSP00000462041.2:p.Ser470=
ENST00000316694.8:c.1410C= MANE Select ENSP00000318868.3:p.Ser470=
ENST00000316694.7:c.1410C= ENSP00000318868.3:p.Ser470=
ENST00000352886.10:c.996C= ENSP00000345881.7:p.Ser332=
ENST00000354098.7:c.1293C= ENSP00000318805.3:p.Ser431=
ENST00000395684.5:n.1733C=
ENST00000580002.5:c.*907C= ENSP00000462043.1:n.*907C=
NM_001281786.1:c.996C= NP_001268715.1:p.Ser332=
NM_004169.4:c.1410C= NP_004160.3:p.Ser470=
NM_148918.2:c.1293C= NP_683718.1:p.Ser431=
XM_005256767.2:c.1410C= XP_005256824.1:p.Ser470=
XM_011523992.1:c.1170C= XP_011522294.1:p.Ser390=
XM_005256767.3:c.1410C= XP_005256824.1:p.Ser470=
XM_011523992.3:c.1170C= XP_011522294.1:p.Ser390=
XM_017024957.1:c.1410C= XP_016880446.1:p.Ser470=
XM_017024958.1:c.1293C= XP_016880447.1:p.Ser431=
XM_024450887.1:c.1170C= XP_024306655.1:p.Ser390=
XM_024450888.1:c.996C= XP_024306656.1:p.Ser332=
XM_024450889.1:c.879C= XP_024306657.1:p.Ser293=
XM_024450890.1:c.756C= XP_024306658.1:p.Ser252=
NM_004169.5:c.1410C= MANE Select NP_004160.3:p.Ser470=
NM_001281786.2:c.996C= NP_001268715.1:p.Ser332=
NM_148918.3:c.1293C= NP_683718.1:p.Ser431=