Canonical Allele Identifier: CA2571826113
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903872C>T , CM000663.2:g.173903872C>T GRCh38
NC_000001.10:g.173873010C>T , CM000663.1:g.173873010C>T GRCh37
NC_000001.9:g.172139633C>T NCBI36
NG_012462.1:g.18507G>A , LRG_577:g.18507G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.*17G>A MANE Select ENSP00000356671.3:n.*17G>A
ENST00000367698.3:c.*17G>A ENSP00000356671.3:n.*17G>A
ENST00000617423.4:c.*17G>A ENSP00000478688.1:n.*17G>A
NM_000488.3:c.*17G>A , LRG_577t1:c.*17G>A NP_000479.1:n.*17G>A
XM_005245198.2:c.*17G>A XP_005245255.1:n.*17G>A
NM_001365052.1:c.*17G>A NP_001351981.1:n.*17G>A
NM_000488.4:c.*17G>A MANE Select NP_000479.1:n.*17G>A
NM_001365052.2:c.*17G>A NP_001351981.1:n.*17G>A
NM_001386302.1:c.*17G>A NP_001373231.1:n.*17G>A
NM_001386303.1:c.*17G>A NP_001373232.1:n.*17G>A
NM_001386304.1:c.*17G>A NP_001373233.1:n.*17G>A
NM_001386305.1:c.*17G>A NP_001373234.1:n.*17G>A
NM_001386306.1:c.*17G>A NP_001373235.1:n.*17G>A
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