Canonical Allele Identifier: CA398629261

Gene: SHMT1

Linked Data

• MyVariant Identifiers: chr17:g.18232101G>T (hg19) ; chr17:g.18328787G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18328787G>T , CM000679.2:g.18328787G>T	GRCh38
NC_000017.10:g.18232101G>T , CM000679.1:g.18232101G>T	GRCh37
NC_000017.9:g.18172826G>T	NCBI36
NG_017111.1:g.39756C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000583780.2:c.1415C>A	ENSP00000462041.2:p.Ala472Asp
ENST00000316694.8:c.1415C>A MANE Select	ENSP00000318868.3:p.Ala472Asp
ENST00000316694.7:c.1415C>A	ENSP00000318868.3:p.Ala472Asp
ENST00000352886.10:c.1001C>A	ENSP00000345881.7:p.Ala334Asp
ENST00000354098.7:c.1298C>A	ENSP00000318805.3:p.Ala433Asp
ENST00000395684.5:n.1738C>A
ENST00000580002.5:c.*912C>A	ENSP00000462043.1:n.*912C>A
NM_001281786.1:c.1001C>A	NP_001268715.1:p.Ala334Asp
NM_004169.4:c.1415C>A	NP_004160.3:p.Ala472Asp
NM_148918.2:c.1298C>A	NP_683718.1:p.Ala433Asp
XM_005256767.2:c.1415C>A	XP_005256824.1:p.Ala472Asp
XM_011523992.1:c.1175C>A	XP_011522294.1:p.Ala392Asp
XM_005256767.3:c.1415C>A	XP_005256824.1:p.Ala472Asp
XM_011523992.3:c.1175C>A	XP_011522294.1:p.Ala392Asp
XM_017024957.1:c.1415C>A	XP_016880446.1:p.Ala472Asp
XM_017024958.1:c.1298C>A	XP_016880447.1:p.Ala433Asp
XM_024450887.1:c.1175C>A	XP_024306655.1:p.Ala392Asp
XM_024450888.1:c.1001C>A	XP_024306656.1:p.Ala334Asp
XM_024450889.1:c.884C>A	XP_024306657.1:p.Ala295Asp
XM_024450890.1:c.761C>A	XP_024306658.1:p.Ala254Asp
NM_004169.5:c.1415C>A MANE Select	NP_004160.3:p.Ala472Asp
NM_001281786.2:c.1001C>A	NP_001268715.1:p.Ala334Asp
NM_148918.3:c.1298C>A	NP_683718.1:p.Ala433Asp