Canonical Allele Identifier: CA358952532

Gene: MTNR1A

Linked Data

• MyVariant Identifiers: chr4:g.187455309A>G (hg19) ; chr4:g.186534155A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186534155A>G , CM000666.2:g.186534155A>G	GRCh38
NC_000004.11:g.187455309A>G , CM000666.1:g.187455309A>G	GRCh37
NC_000004.10:g.187692303A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000703170.1:c.587T>C	ENSP00000515216.1:p.Phe196Ser
ENST00000307161.5:c.587T>C MANE Select	ENSP00000302811.5:p.Phe196Ser
ENST00000509111.2:c.147+21027T>C
NM_005958.3:c.587T>C	NP_005949.1:p.Phe196Ser
XM_011532002.1:c.332T>C	XP_011530304.1:p.Phe111Ser
XR_939589.1:n.1982-11489A>G
XR_939590.1:n.162-11489A>G
NM_005958.4:c.587T>C MANE Select	NP_005949.1:p.Phe196Ser
XM_011532002.3:c.332T>C	XP_011530304.1:p.Phe111Ser
XR_939589.2:n.1982-11489A>G
XR_939590.2:n.162-11489A>G