Canonical Allele Identifier: CA528685113

Gene: FLVCR1

Linked Data

• dbSNP Id: rs1208557401
• gnomAD v2: 1-213056893-T-TTTG
• gnomAD v3: 1-212883551-T-TTTG
• gnomAD v4: 1-212883551-T-TTTG
• MyVariant Identifiers: chr1:g.213056893_213056894insTTG (hg19) ; chr1:g.212883551_212883552insTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883551_212883552insTTG , CM000663.2:g.212883551_212883552insTTG	GRCh38
NC_000001.10:g.213056893_213056894insTTG , CM000663.1:g.213056893_213056894insTTG	GRCh37
NC_000001.9:g.211123516_211123517insTTG	NCBI36
NG_028131.1:g.30297_30298insTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1092+113_1092+114insTTG MANE Select	ENSP00000355938.4:n.1092+113_1092+114insTTG
ENST00000366971.8:c.1092+113_1092+114insTTG	ENSP00000355938.4:n.1092+113_1092+114insTTG
ENST00000419102.1:c.488+113_488+114insTTG
ENST00000474693.1:n.317+113_317+114insTTG
ENST00000483790.1:n.30+113_30+114insTTG
NM_014053.3:c.1092+113_1092+114insTTG	NP_054772.1:n.1092+113_1092+114insTTG
XM_011509446.1:c.1092+113_1092+114insTTG	XP_011507748.1:n.1092+113_1092+114insTTG
XR_247024.1:n.1266+113_1266+114insTTG
XR_426771.1:n.1393+113_1393+114insTTG
XM_011509446.3:c.1092+113_1092+114insTTG	XP_011507748.1:n.1092+113_1092+114insTTG
XR_247024.3:n.1266+113_1266+114insTTG
NM_014053.4:c.1092+113_1092+114insTTG MANE Select	NP_054772.1:n.1092+113_1092+114insTTG