Canonical Allele Identifier: CA420148637

Gene: SRGAP2C SRGAP2-AS1

Linked Data

• dbSNP Id: rs2580520
• gnomAD v2: 1-121112052-C-G
• gnomAD v3: 1-121370191-C-G
• gnomAD v4: 1-121370191-C-G
• MyVariant Identifiers: chr1:g.121112052C>G (hg19) ; chr1:g.121370191C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.121370191C>G , CM000663.2:g.121370191C>G	GRCh38
NC_000001.10:g.121112052C>G , CM000663.1:g.121112052C>G	GRCh37

Transcript Alleles

HGVS	Amino-acid change
ENST00000367123.8:c.487-3780C>G (SRGAP2C) MANE Select	ENSP00000478290.1:n.487-3780C>G
ENST00000304465.7:c.28-3780C>G (SRGAP2C)	ENSP00000483477.1:n.28-3780C>G
ENST00000367123.7:c.487-3780C>G (SRGAP2C)	ENSP00000478290.1:n.487-3780C>G
NM_001271872.1:c.487-3780C>G (SRGAP2C)	NP_001258801.1:n.487-3780C>G
NR_104189.1:n.330-7303G>C (SRGAP2-AS1)
XM_005277497.2:c.487-3780C>G (SRGAP2C)	XP_005277554.1:n.487-3780C>G
XM_005277498.2:c.28-3780C>G (SRGAP2C)	XP_005277555.1:n.28-3780C>G
XM_005277499.3:c.28-3780C>G (SRGAP2C)	XP_005277556.1:n.28-3780C>G
XM_011542015.1:c.394-3780C>G (SRGAP2C)	XP_011540317.1:n.394-3780C>G
XM_011542016.1:c.487-3780C>G (SRGAP2C)	XP_011540318.1:n.487-3780C>G
NM_001271872.2:c.487-3780C>G (SRGAP2C)	NP_001258801.1:n.487-3780C>G
NM_001329984.1:c.487-3780C>G (SRGAP2C)	NP_001316913.1:n.487-3780C>G
XM_005277499.4:c.28-3780C>G (SRGAP2C)	XP_005277556.1:n.28-3780C>G
XM_011542015.3:c.394-3780C>G (SRGAP2C)	XP_011540317.1:n.394-3780C>G
XM_017002149.1:c.28-3780C>G (SRGAP2C)	XP_016857638.1:n.28-3780C>G
XR_001737372.1:n.1187-3780C>G (SRGAP2C)
NM_001271872.3:c.487-3780C>G (SRGAP2C)	NP_001258801.1:n.487-3780C>G
NM_001329984.2:c.487-3780C>G (SRGAP2C) MANE Select	NP_001316913.1:n.487-3780C>G