Canonical Allele Identifier: CA375730046

Gene: GRIN1

Linked Data

• MyVariant Identifiers: chr9:g.140061959T>C (hg19) ; chr9:g.137167507T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137167507T>C , CM000671.2:g.137167507T>C	GRCh38
NC_000009.11:g.140061959T>C , CM000671.1:g.140061959T>C	GRCh37
NC_000009.10:g.139181780T>C	NCBI36
NG_011507.1:g.33351T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371553.8:c.2764-267T>C	ENSP00000360608.3:n.2764-267T>C
ENST00000371560.5:c.2653-267T>C	ENSP00000360615.3:n.2653-267T>C
ENST00000371561.8:c.2797T>C MANE Select	ENSP00000360616.3:p.Ser933Pro
ENST00000371546.8:c.2860T>C	ENSP00000360601.4:p.Ser954Pro
ENST00000371550.8:c.2686T>C	ENSP00000360605.4:p.Ser896Pro
ENST00000371553.7:c.2764-267T>C	ENSP00000360608.3:n.2764-267T>C
ENST00000371555.8:c.2749T>C	ENSP00000360610.4:p.Ser917Pro
ENST00000371559.8:c.2590-267T>C	ENSP00000360614.4:n.2590-267T>C
ENST00000371560.4:c.2653-267T>C	ENSP00000360615.3:n.2653-267T>C
ENST00000371561.7:c.2797T>C	ENSP00000360616.3:p.Ser933Pro
ENST00000473811.1:n.277T>C
NM_000832.6:c.2590-267T>C	NP_000823.4:n.2590-267T>C
NM_001185090.1:c.2764-267T>C	NP_001172019.1:n.2764-267T>C
NM_001185091.1:c.2653-267T>C	NP_001172020.1:n.2653-267T>C
NM_007327.3:c.2797T>C	NP_015566.1:p.Ser933Pro
NM_021569.3:c.2686T>C	NP_067544.1:p.Ser896Pro
XM_005266071.2:c.2701-267T>C	XP_005266128.1:n.2701-267T>C
XM_005266072.2:c.2749T>C	XP_005266129.1:p.Ser917Pro
XM_005266073.3:c.2860T>C	XP_005266130.1:p.Ser954Pro
XM_005266071.3:c.2701-267T>C	XP_005266128.1:n.2701-267T>C
XM_005266072.3:c.2749T>C	XP_005266129.1:p.Ser917Pro
XM_005266073.4:c.2860T>C	XP_005266130.1:p.Ser954Pro
NM_007327.4:c.2797T>C MANE Select	NP_015566.1:p.Ser933Pro
NM_000832.7:c.2590-267T>C	NP_000823.4:n.2590-267T>C
NM_001185090.2:c.2764-267T>C	NP_001172019.1:n.2764-267T>C
NM_001185091.2:c.2653-267T>C	NP_001172020.1:n.2653-267T>C
NM_021569.4:c.2686T>C	NP_067544.1:p.Ser896Pro