Canonical Allele Identifier: CA344235777

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097376A>T (hg19) ; chr1:g.202128248A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128248A>T , CM000663.2:g.202128248A>T	GRCh38
NC_000001.10:g.202097376A>T , CM000663.1:g.202097376A>T	GRCh37
NC_000001.9:g.200363999A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.719A>T
ENST00000682545.1:c.*144A>T	ENSP00000508402.1:n.*144A>T
ENST00000682887.1:c.1539A>T	ENSP00000506946.1:n.1539A>T
ENST00000683302.1:c.1069A>T	ENSP00000507885.1:p.Ile357Phe
ENST00000683557.1:c.729A>T	ENSP00000508029.1:p.Thr243=
ENST00000367282.6:c.1138A>T MANE Select	ENSP00000356251.4:p.Ile380Phe
ENST00000367282.5:c.1138A>T	ENSP00000356251.4:p.Ile380Phe
NM_004767.3:c.1138A>T	NP_004758.3:p.Ile380Phe
XM_011510158.1:c.577A>T	XP_011508460.1:p.Ile193Phe
NM_004767.4:c.1138A>T	NP_004758.3:p.Ile380Phe
XM_011510158.2:c.577A>T	XP_011508460.1:p.Ile193Phe
NM_004767.5:c.1138A>T MANE Select	NP_004758.3:p.Ile380Phe