Canonical Allele Identifier: CA11177691

Gene: DCDC2C

Linked Data

• dbSNP Id: rs11677370
• gnomAD v2: 2-3841420-T-A
• gnomAD v3: 2-3793830-T-A
• gnomAD v4: 2-3793830-T-A
• MyVariant Identifiers: chr2:g.3841420T>A (hg19) ; chr2:g.3793830T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3793830T>A , CM000664.2:g.3793830T>A	GRCh38
NC_000002.11:g.3841420T>A , CM000664.1:g.3841420T>A	GRCh37
NC_000002.10:g.3819295T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000399143.9:c.1065+8730T>A MANE Select	ENSP00000382097.4:n.1065+8730T>A
ENST00000399143.7:c.1065+8730T>A	ENSP00000382097.4:n.1065+8730T>A
NM_001287444.1:c.1065+8730T>A	NP_001274373.1:n.1065+8730T>A
XM_006711894.2:c.1065+8730T>A	XP_006711957.1:n.1065+8730T>A
XM_011510388.1:c.1158+8730T>A	XP_011508690.1:n.1158+8730T>A
XM_011510390.1:c.1158+8730T>A	XP_011508692.1:n.1158+8730T>A
XM_011510392.1:c.1029+8730T>A	XP_011508694.1:n.1029+8730T>A
XR_922682.1:n.1312+8730T>A
XR_922683.1:n.1312+8730T>A
XR_922684.1:n.1312+8730T>A
NM_001365580.1:c.663+8730T>A	NP_001352509.1:n.663+8730T>A
XM_006711894.4:c.1065+8730T>A	XP_006711957.1:n.1065+8730T>A
XR_001738920.2:n.1065+8730T>A
XR_001738921.2:n.1065+8730T>A
NM_001287444.2:c.1065+8730T>A MANE Select	NP_001274373.1:n.1065+8730T>A
NM_001365580.2:c.663+8730T>A	NP_001352509.1:n.663+8730T>A